An anthropometric study of males with the Fragile‐X syndrome
- 1 January 1984
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 17 (1) , 159-174
- https://doi.org/10.1002/ajmg.1320170110
Abstract
Anthropometric methods were used to examine 18 males 18 to 69 years old with the Fragile-X syndrome. Thirteen of 15 subjects had macroorchidism. The average height of the individuals with the Fragile-X was less than that of published standards. Seventeen of the 18 subjects had absolute or relative macrocephaly, and two-thirds of the subjects were dolichocephalic. For the group as a whole, facial and ear lengths were increased, and facial breadth, hand length, and foot length were decreased. It is suggested that relationships between various measurements of an individual may be more important than any single measurements for conveying the characteristic appearance of an individual with the Fragile-X syndrome.Keywords
This publication has 12 references indexed in Scilit:
- Macroorchidism, Mental Retardation, and the Fragile XNew England Journal of Medicine, 1981
- X-linked mental retardation with the fragile X. A study of 15 familiesHuman Genetics, 1981
- X-linked mental retardation, macro-orchidism, and the Xq27 fragile siteThe Journal of Pediatrics, 1980
- Familial X-linked mental retardation with a marker X chromosome and its relationship to macro-orchidismClinical Genetics, 1980
- X‐linked mental retardation: A study of 7 familiesAmerican Journal of Medical Genetics, 1980
- X‐linked mental retardation: Renpenning revisitedAmerican Journal of Medical Genetics, 1980
- Significance of phenotypic and chromosomal abnormalities in X‐linked mental retardation (Martin‐Bell or Renpenning syndrome)American Journal of Medical Genetics, 1980
- More on Marker X Chromosomes, Mental Retardation and Macro-OrchidismNew England Journal of Medicine, 1979
- X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28Human Genetics, 1979
- Inherited congenital normofunctional testicular hyperplasia and mental deficiencyHuman Genetics, 1976