Literature DB >> 2545811

[Prenatal diagnosis of X-linked adrenal hypoplasia associated with glycerol kinase deficiency].

G Malpuech1, B Dastugue, G Giraud, P Jouanel, P Vanlieferinghen, H Carla.   

Abstract

We report a case of X-linked adrenal hypoplasia associated with glycerol kinase deficiency in a boy. Cytogenetic studies and X-linked probes did not demonstrate deletion at Xp21. These probes are not informative enough to be used in prenatal diagnosis. This diagnosis was achieved by glycerol concentration assay in amniotic fluid and by maternal plasma estriol assay.

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Year:  1989        PMID: 2545811

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  2 in total

1.  Complex glycerol kinase deficiency: an X-linked disorder associated with adrenal hypoplasia congenita.

Authors:  Arvind Sehgal; Jacqueline Stack
Journal:  Indian J Pediatr       Date:  2005-01       Impact factor: 1.967

Review 2.  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

  2 in total

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