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Синдром поренцефалії-гіпоплазії мозочка-внутрішніх вад розвитку

ORPHA:2941· ICD-10 Q87.8· Porencephaly-cerebellar hypoplasia-internal malformations syndrome

Визначення(English summary)

Porencephaly-cerebellar hypoplasia-internal malformations syndrome is rare central nervous system malformation syndrome characterized by bilateral porencephaly, absence of the septum pellucidum and cerebellar hypoplasia with absent vermis. Additionally, dysmorphic facial features (hypertelorism, epicanthic folds, high arched palate, prominent metopic suture), macrocephaly, corneal clouding, situs inversus, tetralogy of Fallot, atrial septal defects and/or seizures have been observed.

Поширеність
<1 / 1 000 000
Вік початку
Antenatal, Neonatal