Pediatric pointed and toe syndrome
Acrocephalosyndactyly syndrome in children is a rare autosomal dominant hereditary disease with an incidence rate of 1 / 160,000, which is mainly manifested in abnormalities of the skull and facial bones, and is accompanied by digits ) Malformed set of symptoms. Also known as Apert syndrome, pointed and toe deformity, and syndactylic oxycephaly syndrome.
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