Literature DB >> 8275570

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

M G Butler1, R Pratesi, M S Watson, W R Breg, D N Singh.   

Abstract

Anthropometric and craniofacial profile patterns indicating the percent difference from the overall mean were developed on 34 physical parameters with 31 white, mentally retarded males (23 adults and 8 children) with the fra(X) syndrome matched for age with 31 white, mentally retarded males without a known cause of their retardation. The fra(X) syndrome males consistently showed larger dimensions for all anthropometric variables, with significant differences for height, sitting height, arm span, hand length, middle finger length, hand breadth, foot length, foot breadth, and testicular volume. A craniofacial pattern did emerge between the two groups of mentally retarded males, but with overlap of several variables. Significant differences were noted for head circumference, head breadth, lower face height, bizygomatic diameter, inner canthal distance, ear length and ear width, with the fra(X) syndrome males having larger head dimensions (head circumference, head breadth, head length, face height and lower face height), but smaller measurements for minimal frontal diameter, bizygomatic diameter, bigonial diameter, and inner canthal distance. Several significant correlations were found with the variables for both mentally retarded males with and without the fra(X) syndrome. In a combined anthropometric and craniofacial profile of 19 variables comparing 26 white fra(X) syndrome males (13 with high expression (> 30%) and 13 with low expression (< 30%), but matched for age), a relatively flat profile was observed with no significant differences for any of the variables. Generally, fra(X) syndrome males with increased fragile X chromosome expression have larger amplifications of the CGG trinucleotide repeat of the FMR-1 gene. No physical differences were detectable in our study between fra(X) males with high expression and apparently larger amplifications of the CGG trinucleotide repeats compared with those patients with low expression. Our research illustrates the use of anthropometry in identifying differences between mentally retarded males with or without the fra(X) syndrome and offers a comprehensive approach for screening males for the fra(X) syndrome and selecting those individuals for cytogenetic and/or molecular genetic testing.

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Year:  1993        PMID: 8275570      PMCID: PMC5464415          DOI: 10.1111/j.1399-0004.1993.tb03863.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  27 in total

1.  Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.

Authors:  G R Sutherland; A Gedeon; L Kornman; A Donnelly; R W Byard; J C Mulley; E Kremer; M Lynch; M Pritchard; S Yu
Journal:  N Engl J Med       Date:  1991-12-12       Impact factor: 91.245

2.  Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.

Authors:  M G Butler; G A Allen; J L Haynes; S J Clark
Journal:  Am J Med Genet       Date:  1990-10

3.  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

4.  Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.

Authors:  M G Butler; D N Singh
Journal:  J Intellect Disabil Res       Date:  1993-04

5.  An anthropometric study of males with the fragile-X syndrome.

Authors:  D L Meryash; C E Cronk; B Sachs; P S Gerald
Journal:  Am J Med Genet       Date:  1984-01

6.  Anthropometry in Martin-Bell syndrome.

Authors:  D Z Loesch; M Lafranchi; D Scott
Journal:  Am J Med Genet       Date:  1988 May-Jun

7.  Absence of expression of the FMR-1 gene in fragile X syndrome.

Authors:  M Pieretti; F P Zhang; Y H Fu; S T Warren; B A Oostra; C T Caskey; D L Nelson
Journal:  Cell       Date:  1991-08-23       Impact factor: 41.582

8.  A 15-item checklist for screening mentally retarded males for the fragile X syndrome.

Authors:  M G Butler; T Mangrum; R Gupta; D N Singh
Journal:  Clin Genet       Date:  1991-05       Impact factor: 4.438

9.  Population incidence and segregation ratios in the Martin-Bell syndrome.

Authors:  T P Webb; S E Bundey; A I Thake; J Todd
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

10.  Nonspecific X-linked mental retardation II: the frequency in British Columbia.

Authors:  D S Herbst; J R Miller
Journal:  Am J Med Genet       Date:  1980
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  9 in total

1.  Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.

Authors:  M G Butler; R Pratesi; C L Vnencak-Jones
Journal:  J Intellect Disabil Res       Date:  1995-12

2.  Association between macroorchidism and intelligence in FMR1 premutation carriers.

Authors:  Reymundo Lozano; Scott Summers; Cristina Lozano; Yi Mu; David Hessl; Danh Nguyen; Flora Tassone; Randi Hagerman
Journal:  Am J Med Genet A       Date:  2014-06-05       Impact factor: 2.802

3.  Screen for MAOA mutations in target human groups.

Authors:  D E Schuback; E L Mulligan; K B Sims; E A Tivol; B D Greenberg; S F Chang; S L Yang; Y C Mau; C Y Shen; M S Ho; N H Yang; M G Butler; S Fink; C E Schwartz; F Berlin; X O Breakefield; D L Murphy; Y P Hsu
Journal:  Am J Med Genet       Date:  1999-02-05

4.  FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDY.

Authors:  Merlin G Butler
Journal:  J Tenn Acad Sci       Date:  1998 Jul-Oct

Review 5.  Unstable mutations in the FMR1 gene and the phenotypes.

Authors:  Danuta Loesch; Randi Hagerman
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

6.  Fragile X syndrome: panoramic radiographic evaluation of dental anomalies, dental mineralization stage, and mandibular angle.

Authors:  Aida Sabbagh-Haddad; Denise Sabbagh Haddad; Edgard Michel-Crosato; Emiko Saito Arita
Journal:  J Appl Oral Sci       Date:  2016 Sep-Oct       Impact factor: 2.698

7.  Fmr1-Deficiency Impacts Body Composition, Skeleton, and Bone Microstructure in a Mouse Model of Fragile X Syndrome.

Authors:  Antoine Leboucher; Patricia Bermudez-Martin; Xavier Mouska; Ez-Zoubir Amri; Didier F Pisani; Laetitia Davidovic
Journal:  Front Endocrinol (Lausanne)       Date:  2019-10-02       Impact factor: 5.555

8.  Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review.

Authors:  Merlin G Butler; Waheeda A Hossain; Jacob Steinle; Harry Gao; Eleina Cox; Yuxin Niu; May Quach; Olivia J Veatch
Journal:  Int J Mol Sci       Date:  2022-08-13       Impact factor: 6.208

9.  Facial metrics in children with corticotrophin-producing pituitary adenomas suggest abnormalities in midface development.

Authors:  Margaret F Keil; Constantine A Stratakis
Journal:  J Pediatr Endocrinol Metab       Date:  2009-01       Impact factor: 1.634

  9 in total

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