Literature DB >> 3177440

Anthropometry in Martin-Bell syndrome.

D Z Loesch1, M Lafranchi, D Scott.   

Abstract

Thirty anthropometric measurements were analyzed in 147 adults with Martin-Bell syndrome (MBS) (56 men and 91 women) and in a random sample of 108 normal women and 111 men. Results of the univariate comparison of the age, height, or weight-adjusted variables between MBS and normal individuals of either sex indicated that a decrease in stature, in upper limb length, and in upper face height, and an increase in jaw length, chest circumference, and waist width occurred in both affected men and in heterozygous women. While the increase in ear height and breadth and in hypermobility of finger joints and decrease in palm width and bigonial diameter occurred only in affected men, increased bispinal and bitrochanteric diameters, upper arm circumference, and palm and wrist widths were characteristic deviations in heterozygous women. Multivariate analysis in the form of principal components showed some differences in the pattern of interrelationships in individual measures between MBS and normal individuals. In particular, and in contrast with both normal groups, height and weight tended to load on separate components (as did head and midfacial measures) in MBS individuals. A discriminant function based on all body measurements included in this study resulted in almost complete separation of discriminant scores of normal from those of MBS men and in good separation of the scores from normal and heterozygous women. Classification rates based on these functions were from 95% in men to 85% in women. These already high classification rates may be further improved mainly by enlarging the samples and including some other category of traits such as dermatoglyphic measurements.

Entities:  

Mesh:

Year:  1988        PMID: 3177440     DOI: 10.1002/ajmg.1320300113

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  12 in total

1.  Genetic counselling.

Authors:  M Barker; D Livingstone
Journal:  Occas Pap R Coll Gen Pract       Date:  1990-11

2.  Fixed and random effects in the variation of the finger ridge count: a study of fragile-X families.

Authors:  D Z Loesch; R M Huggins
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

3.  Standards for selected anthropometric measurements in males with the fragile X syndrome.

Authors:  M G Butler; A Brunschwig; L K Miller; R J Hagerman
Journal:  Pediatrics       Date:  1992-06       Impact factor: 7.124

4.  General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutation.

Authors:  B B de Vries; H Robinson; I Stolte-Dijkstra; C V Tjon Pian Gi; P F Dijkstra; J van Doorn; D J Halley; B A Oostra; G Turner; M F Niermeijer
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

5.  Between-generation differences in ascertainment and penetrance: relevance to genetic hypotheses in fragile X.

Authors:  D Z Loesch; L J Sheffield; D A Hay
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

6.  Anthropometric comparison of mentally retarded males with and without the fragile X syndrome.

Authors:  M G Butler; G A Allen; J L Haynes; D N Singh; M S Watson; W R Breg
Journal:  Am J Med Genet       Date:  1991 Feb-Mar

7.  Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome.

Authors:  M G Butler; R Pratesi; M S Watson; W R Breg; D N Singh
Journal:  Clin Genet       Date:  1993-09       Impact factor: 4.438

8.  Genotype-phenotype relationships in fragile X syndrome: a family study.

Authors:  D Z Loesch; R Huggins; D A Hay; A K Gedeon; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

9.  Craniofacial characteristics of fragile X syndrome in mouse and man.

Authors:  Inge Heulens; Michael Suttie; Andrei Postnov; Nora De Clerck; Concetta S Perrotta; Teresa Mattina; Francesca Faravelli; Francesca Forzano; R Frank Kooy; Peter Hammond
Journal:  Eur J Hum Genet       Date:  2012-12-05       Impact factor: 4.246

Review 10.  The fragile X syndrome.

Authors:  B B de Vries; D J Halley; B A Oostra; M F Niermeijer
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

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