White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome

Orpha code: 3207OMIM code:

Definicja

A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by severe white matter hypoplasia, corpus callosum agenesis or extreme hypoplasia, severe intellectual disability, failure to thrive and minor midline facial dysmorphism (including hypertelorism, broad nasal root, micrognathia). There have been no further descriptions in the literature since 1993.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Curatolo-Cilio-Pessagno syndrome
Zespół Curatolo, Cilio i Pessagno
Kod ORPHA
3207
Kod OMIM
-
Kod ICD10
Q87.0
Kod ICD11
-

No additional description.

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