Vincenzina Care
  • Art work
  • How to order a doll
  • Available doll painters
  • Reborn kits
    • First Reborn Kit "Stanley Oliver" with Down syndrome
    • Second Reborn Kit "Nino" with Achondroplasia Dwarfism
    • Third reborn Kit "Gianna & Giulia" with Diprosopus
    • Forth Reborn Kit "Gounchin"
  • Chenza dolls Merchandise
    • Chenza dolls shop
    • Redbubble store
    • Teespring store
    • Buy my book!
  • Custom work
    • Mini babies
    • Paper dolls
    • Chenza Dolls
    • Animal sculptures
    • Pumpkins/Butter Sculptures
  • chenza's imaginarium
  • Media
  • About
  • Contact

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Lily and Lilac- 2022 

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Gordo -2022

Genevieve-2022

Genevieve-2022

Lily and Lilac- 2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Hayden & Harvey-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Genevieve-2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Lily and Lilac- 2022

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022)

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Reggie (2022)

Reggie (2022)

Reggie (2022)

Reggie (2022)

Reggie (2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

 (2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Temperance- 2022

Temperance- 2022

Temperance- 2022

Temperance- 2022

Lawrence & Leo cranio- facial duplication 

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

 

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

Ray-2022

Ray-2022

Ray-2022

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray-2022

Ray-2022

Ray-2022

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

Orion- 2022 

Orion- 2022

Orion- 2022

Trés- 

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Trés- 

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés-

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- 

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés-

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés-

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- 

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés-

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Orion- 2022

Trés- 

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

  cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Page with Progeria 

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth. 

Page with Progeria

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth. 

Page with Progeria

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth. 

Page with Progeria

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth.

Kayla -2022

Kayla -2022

Kayla -2022

Kayla -2022

Kayla -2022

Kayla -2022

Orion-2022

Orion-2022

Lawrence & Leo cranio- facial duplication

A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Ray 2022 

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Yanni and Nico

cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Natasha with albinism

The term albinism typically refers to oculocutaneous (ok-u-low-ku-TAY-nee-us) albinism (OCA) — a group of inherited disorders where there is little or no production of the pigment melanin. The type and amount of melanin your body produces determines the color of your skin, hair and eyes.

(2022)

Kayla-2022

Kayla-2022

Kayla-2022

Kayla-2022

Kayla-2022

Kayla-2022

Page with Progeria

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth.

Page with Progeria

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear normal at birth.

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Nila with Waardenburg syndrome

-Waardenburg syndrome (WS) is an auditory-pigmentary syndrome caused by a deficiency of melanocytes and other neural crest-derived cells. Depending on a variety of symptoms associated with the auditory-pigmentary symptoms, WS is classified into four types: WS type 1 (WS1), WS2, WS3, and WS4.(2022) 

Trés- cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Trés- cranio Facial duplication A craniofacial duplication or diprosopus is an unusual variant of conjoined twinning. The reported incidence is one in 180,000-15 million births and 35 cases have been reported till date. The phenotype is wide, with the partial duplication of a few facial structures to complete dicephalus.

 

Reggie-2022

Reggie-2022

Reggie-2022

Reggie-2022

Reggie-2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Felix doll with Down syndrome 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Graziella 2022

Jayde 2022