A large kindred with X‐linked mental retardation, marker X and macroorchidism
- 1 January 1984
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 17 (1) , 145-157
- https://doi.org/10.1002/ajmg.1320170109
Abstract
Thirty‐eight members of a black kindred with mental retardation and the Marker X were studied. Ten of 14 affected males, 6 of 6 affected females, 18 carriers or possible carriers, and 7 normal males were examined. Eight of 9 affected males who could be measured had macroorchidism, but their ears and mandibles were not prominent. No distinct facies were evident, although minor anomalies, such as a slight pectus, were present in some. Clinical diagnosis in the absence of a strongly positive family history may be even more difficult among prepubertal black children than in whites. The risk of retardation among children of carriers was estimated at 20–40%.Keywords
This publication has 3 references indexed in Scilit:
- Brief report: Linkage between G6PD and fragile‐X syndromeAmerican Journal of Medical Genetics, 1983
- Fragile X-Linked Mental RetardationAmerican Journal of Diseases of Children, 1982
- X-Linked Mental Retardation with a Fragile Site in Xq and an Inversion of Chromosome No. 9Human Heredity, 1981