Literature DB >> 709903

Autosomal recessive inheritance of metaphyseal dysplasia (Pyle disease).

M S Raad, P Beighton.   

Abstract

Two young adults with Pyle disease have been investigated in a large Afrikaner kindred in South Africa. Consanguinity was present in the family, and it is likely that the condition was inherited as an autosomal recessive. This contention is supported by the radiographic demonstration of minor degrees of widening of the distal femora in obligatory and potentially heterozygous relatives. Apart from genu valgus of moderate degree, the patients enjoyed good health and their gross radiographic skeletal abnormalities contrasted with the innocuous clinical presentation. Differentiation of Pyle disease from the autosomal dominant and autosomal recessive forms of cranio-metaphyseal dysplasia is of prognostic importance in view of the potentially serious complications in these latter disorders.

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Year:  1978        PMID: 709903     DOI: 10.1111/j.1399-0004.1978.tb02142.x

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


  3 in total

1.  Craniometaphyseal dysplasia (CMD), autosomal dominant form.

Authors:  P Beighton
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

2.  A novel sequence variant in SFRP4 causing Pyle disease.

Authors:  Chelna Galada; Hitesh Shah; Anju Shukla; Katta M Girisha
Journal:  J Hum Genet       Date:  2017-01-19       Impact factor: 3.172

3.  Metaphyseal dysplasia associated with chronic facial nerve palsy.

Authors:  Loucas Christodoulou; Efterpi Pavlidou; Cristina Spyridou; Simon Eccles; Alistair Calder; Kshitij Mankad; Maria Kinali
Journal:  Childs Nerv Syst       Date:  2016-02-04       Impact factor: 1.475

  3 in total

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