White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome

Orpha code: 3207OMIM code:

Definition

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
Classification

Malformation syndrome

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

No additional description.

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