Literature DB >> 6315281

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs.

W O Renier, F A Nabben, T W Hustinx, J H Veerkamp, B J Otten, H J Ter Laak, B G Ter Haar, F J Gabreëls.   

Abstract

A family is described with three male sibs suffering from congenital adrenal hypoplasia (CAH). In the two surviving brothers the disease is clinically further characterized by a Duchenne type muscular dystrophy, growth failure and severe mental retardation. Laboratory investigations revealed deficient activities of gonadotrophin and glycerol kinase. The clinical, biochemical and genetic findings in ths exceptional family are reported and discussed.

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Year:  1983        PMID: 6315281     DOI: 10.1111/j.1399-0004.1983.tb00078.x

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


  10 in total

1.  Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases.

Authors:  A Kohlschütter; H P Willig; D Schlamp; K Kruse; E R McCabe; H J Schäfer; G Beckenkamp; R Rohkamm
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

2.  Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Authors:  M A Musarella; A Burghes; L Anson-Cartwright; M M Mahtani; R Argonza; L C Tsui; R Worton
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  Short stature: a common feature in Duchenne muscular dystrophy.

Authors:  U Eiholzer; E Boltshauser; D Frey; L Molinari; M Zachmann
Journal:  Eur J Pediatr       Date:  1988-08       Impact factor: 3.183

Review 4.  Recently recognized chromosomal defects of clinical importance.

Authors:  M Pembrey; M Baraitser
Journal:  Postgrad Med J       Date:  1986-02       Impact factor: 2.401

5.  Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.

Authors:  A Clarke; S H Roberts; N S Thomas; A Whitfield; J Williams; P S Harper
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

Review 6.  On the nature of the Duchenne muscular dystrophy locus: a portion of a complex of related gene clusters of recent pseudoautosomal origin?

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1988-06       Impact factor: 3.396

Review 7.  Isolated and contiguous glycerol kinase gene disorders: a review.

Authors:  D R Sjarif; J K Ploos van Amstel; M Duran; F A Beemer; B T Poll-The
Journal:  J Inherit Metab Dis       Date:  2000-09       Impact factor: 4.982

8.  Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Authors:  U Francke; J F Harper; B T Darras; J M Cowan; E R McCabe; A Kohlschütter; W K Seltzer; F Saito; J Goto; J P Harpey
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

9.  Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.

Authors:  D E Wilcox; A Cooke; J Colgan; E Boyd; D A Aitken; L Sinclair; L Glasgow; J B Stephenson; M A Ferguson-Smith
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

10.  Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.

Authors:  M H Hofker; A A Bergen; M I Skraastad; E Bakker; U Francke; B Wieringa; J Bartley; G J van Ommen; P L Pearson
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

  10 in total

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