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
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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
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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
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Graziella 2022
Jayde 2022
Jayde 2022
Jayde 2022
Jayde 2022