Literature DB >> 1956063

Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?

W Reardon1, C M Hall, M J Dillon, M Baraitser.   

Abstract

A brother and sister are presented with unusual facies, bilateral mixed hearing loss, mental retardation, and widespread radiological abnormalities. The clinical and radiological evidence for and against the two most likely diagnoses of frontometaphyseal dysplasia and craniometaphyseal dysplasia is considered.

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Mesh:

Year:  1991        PMID: 1956063      PMCID: PMC1015795          DOI: 10.1136/jmg.28.9.622

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissue.

Authors:  D M Danks; V Mayne; R K Hall; M C McKinnon
Journal:  Am J Dis Child       Date:  1972-03

2.  Frontometaphyseal dysplasia. A new syndrome.

Authors:  R J Gorlin; M M Cohen
Journal:  Am J Dis Child       Date:  1969-09

3.  Frontometaphyseal dysplasia--evidence for X-linked inheritance.

Authors:  R J Gorlin; R B Winter
Journal:  Am J Med Genet       Date:  1980

4.  Craniofacial surgery in craniometaphyseal dysplasia.

Authors:  D R Millard; D O Maisels; J H Batstone; B W Yates
Journal:  Am J Surg       Date:  1967-05       Impact factor: 2.565

5.  Frontometaphyseal Dysplasia. Evidence for dominant inheritance.

Authors:  L Weiss; W A Reynolds; R T Szymanowski
Journal:  Am J Dis Child       Date:  1976-03
  5 in total

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