Monosomy 10 qter
- 1 January 1979
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 47 (3) , 233-237
- https://doi.org/10.1007/bf00321014
Abstract
An 11-year-old girl with 10q26qter deletion is described and compared with another patient reported in the literature. The most characteristic features of monosomy 10qter seem to be: severe mental retardation; growth retardation; microcephaly; and facial dysmorphism with a long and triangular facies, a broad and prominent nasal bridge, a poorly developed tip of the nose, a short philtrum, and flattened angles of the mandible. Several of these features are opposed in type and countertype to features of trisomy 10qter.Keywords
This publication has 4 references indexed in Scilit:
- Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosomeHuman Genetics, 1978
- Ring 10 chromosome: 46,XX,r10(p15q26)Human Genetics, 1978
- Partial deletion 10qHuman Genetics, 1978
- Physical retardation is associated with ring chromosome mosaicism: 46, XX,r(10)/45, XX,10 minus.Journal of Medical Genetics, 1977