Zespół N

Kod Orpha: 2608Kod OMIM: 310465

Definicja

A rare, fatal multiple congenital anomalies/dysmorphic syndrome characterized by facial dysmorphism (incl. dolichocephaly/scaphocephaly, high frontal hairline, laterally overlapping upper eyelids, hypertelorism, prominent eyelashes, deep-set eyes, macrocornea, nystagmus, dysplastic ears, abnormal auricles, prominent nasal bridge, dental dysplasia), visual impairment, deafness, seizures, generalized skeletal dysplasia, high fingerprint ridge count, cryptorchidism, hypospadias, spasticity and severe intellectual disability. An increased chromosome breakage and a fatal lymphoid malignancy have been reported. There has been no further description in the literature since 1974.

Dane
Klasyfikacja

Zespół wad wrodzonych

Kod ORPHA
2608
Kod OMIM
310465
Kod ICD10
Q87.8
Kod ICD11
LD2H.Y

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