LD40.1
Complete trisomy 13
Trissomia 13 completa
CategoryDefinition
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
Index Terms
Complete trisomy 13Patau syndromecomplete trisomy 13 syndromed1 trisomyd1 trisomy syndromed>1< trisomy syndromepatautrisomy 13trisomy 13 syndromechromosome 13 trisomyabnormal autosomes 13Complete trisomy 13, meiotic non-disjunctiontrisomy 13, meiotic nondisjunctiontrisomy 13 syndrome, meiotic nondisjunctionComplete trisomy 13, translocationpartial trisomy 13 in patau syndrometranslocation trisomy 13translocation trisomy 13 syndrometranslocation trisomy 13 chromosome