Trisomy 13

Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.

Also known as: Patau syndrome, Patau's syndrome, Trisomy 13 Syndrome, trisomy 13, trisomy type 13, D trisomy syndrome (formerly), D1 trisomy, chromosome 13, trisomy 13 complete

18 clinical trials for this condition and its sub-types, 4 tagged with Trisomy 13 itself.