Clinical features and reproductive patterns in fragile X female heterozygotes.
- 1 June 1988
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 25 (6) , 407-414
- https://doi.org/10.1136/jmg.25.6.407
Abstract
Clinical findings are presented on 113 fragile X female heterozygotes from 44 families, based on physical examination, behavioural assessment, and reproductive history. In 85% of a subsample of 92 adult females non-verbal IQ score derived from the Block Design test was 85 or less. Verbal ability deficits were much less common. Typical facial characteristics, irregular teeth, and hypermobility of finger joints occurred in approximately 40% of adult females, but facial abnormalities were less common in children. Some physical anomalies and the level of intellectual impairment were, in adult carriers, associated with the presence of fragile X sites. The commoner physical anomalies or typical facial characteristics and intellectual abilities differed significantly between the known female heterozygotes and their 40 presumed normal relatives. Frequency of miscarriages was increased in fragile X females; in spite of this, a moderate increase in the number of children has been encountered in female carriers with borderline intellectural impairment. This important problem has genetical implications and needs further investigation. The importance is emphasised of a more detailed clinical examination of the females at risk in fragile X families.This publication has 13 references indexed in Scilit:
- Anthropometry in Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1988
- Individual variation and specific cognitive deficits in the fra(X) syndromeAmerican Journal of Medical Genetics, 1987
- Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra(X) femalesAmerican Journal of Medical Genetics, 1986
- The female and the Fragile X. A study of 144 obligate female carriersAmerican Journal of Medical Genetics, 1986
- Second international workshop on the fragile X and on X‐linked mental retardationAmerican Journal of Medical Genetics, 1986
- Detection of the fragile X chromosome and other fragile sitesClinical Genetics, 1985
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985
- Mutation and selection in the marker (X) syndrome A hypothesisAnnals of Human Genetics, 1984
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984
- Congenital anomalies in the newborninfant, including minor variationsThe Journal of Pediatrics, 1964