Meinecke_syndrome
Porencephaly-cerebellar hypoplasia-internal malformations syndrome
Medical condition
Porencephaly-cerebellar hypoplasia-internal malformations syndrome is a rare autosomal recessive syndrome that mainly affects the central nervous system.[2] It causes cardiac defects, brain anomalies, and craniofacial dysmorphisms.[3][4] It has been reported in a pair of German siblings of the opposite sex born to consanguineous Turkish parents.[5]