Literature DB >> 3442297

Craniofacial variation and growth in the Prader-Labhart-Willi syndrome.

F J Meaney1, M G Butler.   

Abstract

A study of anthropometric variation and craniofacial growth in individuals with the Prader-Labhart-Willi syndrome (PLWS) illustrates the utility of anthropometry in clinical evaluation and research. Anthropometric measurements, including head length and breadth, minimum frontal diameter, and head circumference, were obtained on 38 PLWS individuals (21 with chromosome 15 deletions) with an age range from 2 weeks to 39 years. No anthropometric differences were found between the two chromosome subgroups. A relative deceleration in the growth of certain craniofacial dimensions (head circumference and length) is suggested by the negative correlations between age and Z-scores for the measurements. Raw values for minimum frontal diameter and head breadth were near or below the 5th percentile curve, while almost all values for head length and circumference fell within normal limits. The data support suggestions that dolichocephaly be considered an early diagnostic feature of PLWS. Furthermore, the status of narrow bifrontal diameter as a major feature of PLWS is confirmed.

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Year:  1987        PMID: 3442297      PMCID: PMC5990430          DOI: 10.1002/ajpa.1330740405

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  8 in total

1.  The developing role of anthropologists in medical genetics: anthropometric assessment of the Prader-Labhart-Willi syndrome as an illustration.

Authors:  F J Meaney; M G Butler
Journal:  Med Anthropol       Date:  1989-04

2.  An anthropometric study of 38 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney
Journal:  Am J Med Genet       Date:  1987-02

3.  Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence.

Authors:  B D Hall; D W Smith
Journal:  J Pediatr       Date:  1972-08       Impact factor: 4.406

4.  Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome.

Authors:  H Zellweger; H J Schneider
Journal:  Am J Dis Child       Date:  1968-05

5.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney; C G Palmer
Journal:  Am J Med Genet       Date:  1986-03

6.  Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases.

Authors:  M G Butler; F J Meaney
Journal:  Clin Genet       Date:  1985-07       Impact factor: 4.438

Review 7.  Clinical anthropometry and medical genetics: a compilation of body measurements in genetic and congenital disorders.

Authors:  F J Meaney; L A Farrer
Journal:  Am J Med Genet       Date:  1986-10

8.  Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings.

Authors:  T Reed; M G Butler
Journal:  Clin Genet       Date:  1984-04       Impact factor: 4.438

  8 in total
  6 in total

1.  The developing role of anthropologists in medical genetics: anthropometric assessment of the Prader-Labhart-Willi syndrome as an illustration.

Authors:  F J Meaney; M G Butler
Journal:  Med Anthropol       Date:  1989-04

2.  Development and implementation of electronic growth charts for infants with Prader-Willi syndrome.

Authors:  S Trent Rosenbloom; Merlin G Butler
Journal:  Am J Med Genet A       Date:  2012-08-17       Impact factor: 2.802

3.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

4.  Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects.

Authors:  M G Butler; J L Haynes; F J Meaney
Journal:  Clin Genet       Date:  1991-01       Impact factor: 4.438

5.  Craniofacial and dentoalveolar morphology in individuals with Prader-Willi syndrome: a case-control study.

Authors:  Gisela Vasconcelos; Jo S Stenehjem; Stefan Axelsson; Ronnaug Saeves
Journal:  Orphanet J Rare Dis       Date:  2022-02-22       Impact factor: 4.123

6.  Robustness of Distinctive Facial Features in Prader-Willi Syndrome: A Stereophotogrammetric Analysis and Association with Clinical and Biochemical Markers in Adult Individuals.

Authors:  Claudia Dolci; Antonello E Rigamonti; Annalisa Cappella; Daniele M Gibelli; Graziano Grugni; Diana Caroli; Chiarella Sforza; Alessandro Sartorio
Journal:  Biology (Basel)       Date:  2022-07-30
  6 in total

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