LD40.1
category
Complete trisomy 13
Definition
Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterised by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.
Inclusions
- Patau syndrome
Also indexed as
Complete trisomy 13Complete trisomy 13, meiotic non-disjunctionComplete trisomy 13, translocationPatau syndromeabnormal autosomes 13chromosome 13 trisomycomplete trisomy 13 syndromed1 trisomyd1 trisomy syndromed>1< trisomy syndromepartial trisomy 13 in patau syndromepatautranslocation trisomy 13translocation trisomy 13 chromosometranslocation trisomy 13 syndrometrisomy 13trisomy 13 syndrometrisomy 13 syndrome, meiotic nondisjunctiontrisomy 13, meiotic nondisjunction