Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Helv Paediatr Acta ; 41(6): 509-13, 1986 Mar.
Article in English | MEDLINE | ID: mdl-3583774

ABSTRACT

A new case is presented of partial trisomy 3p in a one-year-old mentally retarded female infant with characteristic craniofacial dysmorphism and rare-faction of the stroma of the iris. The partial trisomy resulted from paternal balanced translocation t(3;6)(p25;p25). A review of the literature revealed that 1. both sexes are equally affected; 2. holoprosencephaly, found in 4 of 45 cases, may be considered the major and most severe anomaly of this syndrome; 3. the life-span of partial trisomy 3p is shorter than generally believed as most patients with severe malformations probably die before karyotype studies are initiated.


Subject(s)
Chromosomes, Human, Pair 3 , Facial Bones/abnormalities , Skull/abnormalities , Trisomy , Abnormalities, Multiple/genetics , Brain/abnormalities , Female , Humans , Infant , Karyotyping , Syndrome
SELECTION OF CITATIONS
SEARCH DETAIL
...