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ALPERT
SYNDROME
Alpert syndrome is a congenital disorder characterized by
malformation of the Hands, feets and skull & face. Babies with Alpert
syndrome are both with a distorted shape of head and face. Children with Alpert
syndrome may here intellectual disability.
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Causes:
· Alpert syndrome
is a genetic condition caused by mutation on a gene. That affect gene is
autosomal dominant: FGFR2.
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Characteristics:
· Craniofacial
anomalies affecting the ears, stapes fixation, fused fingers and toes and spina
bifida.
· Associated with
conductive hearing loss.
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Hearing Loss:
· Conductive
Hearing Loss (Congenital)
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