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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Polydactyly-syndactyly-triphalangism
Filippi syndrome
Filippi syndrome is characterized by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline). So far, less than 25 cases have been reported. Cryptorchidism, polydactyly, and teeth and hair anomalies may also be present. Transmission is autosomal recessive.
This condition has no sub-types.