Sporadic fetal brain disruption sequence

Orpha code: 1665OMIM code:

Definicja

Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
1665
Kod OMIM
-
Kod ICD10
Q02
Kod ICD11
-

No additional description.

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