Zespół dysplazji czołowo-nosowej-rozszczepu nosa-wad kończyny górnej

Kod Orpha: 521308Kod OMIM:

Definition

A rare syndromic frontonasal dysplasia characterized by distinctive facial dysmorphic features including hypertelorism, almond-shaped palpebral fissures, nasal deformity with creased ridge, depressed or absent tip, and asymmetry and partial absence of nasal bones, and downturned corners of the mouth. Additional reported manifestations are limb anomalies (e. g. Poland anomaly, transverse limb agenesis, and anomalies of the hands and feet, such as camptodactyly, oligodactyly, clinodactyly, and syndactyly), frontonasal encephalocele, choanal atresia, congenital renal/cardiac malformations, and corpus callosum agenesis.

Dane
Classification

Zespół wad wrodzonych

ORPHA code
521308
OMIM code
-
ICD10 code
Q87.0
ICD11 code
-

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