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Vol. 68, No. 1, 2007   

Free Abstract     Article (Fulltext)     Article (PDF 170 KB)     

Novel Insights from Clinical Practice

A Novel Missense Mutation in Dax-1 with an Unusual Presentation of X-Linked Adrenal Hypoplasia Congenita
Imran Ahmada, Wendy F. Patersona, Lin Linc, Peter Adlardd, Philippa Duncane, John Tolmieb, John C. Achermannc, Malcolm D.C. Donaldsona

aDepartment of Child Health and
bFerguson-Smith Centre for Clinical Genetics, Royal Hospital for Sick Children, Yorkhill, Glasgow,
cDepartment of Endocrinology, UCL Institute of Child Health, University College London, London,
dStoke Mandeville Hospital, Aylesbury, and
eWessex Regional Genetics Laboratory, Salisbury, UK

Address of Corresponding Author

Horm Res 2007;68:32-37 (DOI: 10.1159/000099835)


 goto top of page Key Words

  • DAX-1
  • NR0B1
  • Adrenal insufficiency
  • Adrenal hypoplasia congenita, X-linked
  • Mineralocorticoid

 goto top of page Abstract

A male presented at age 2.2 years with a 6-week history of intermittent vomiting and hyperpigmentation. Investigations showed salt wasting with hyperkalaemia, a grossly impaired cortisol response to ACTH stimulation, elevated renin and ACTH. Family history revealed that two maternal uncles had died soon after birth. A third uncle failed to thrive during infancy but improved with a course of cortisone, then being untreated until further investigation revealed adrenal insufficiency. A fourth uncle died aged 10 days, with urinary salt loss and hypoplastic adrenal glands at postmortem. Molecular studies on the proband, his mother, maternal grandmother, and surviving uncle showed a novel C to G substitution at nucleotide position 794 (missense mutation T265R) in the DAX1 (NR0B1) gene. The proband has responded well to steroid replacement but has proved sensitive to 9alpha-fludrocortisone treatment, developing hypertension on a dose of 133 µg/m2/day. At 8.8 years he was noted to have testicular volumes of 4 ml, despite no other evidence of secondary sexual development and prepubertal gonadotrophin levels. Novel features of this family include a novel DAX1 mutation, marked variability in age of presentation, hypertension on 'standard' doses of 9alpha-fludrocortisone and mild testicular enlargement.

Copyright © 2007 S. Karger AG, Basel


 goto top of page Author Contacts

Dr. Malcolm D.C. Donaldson
Department of Child Health
Royal Hospital for Sick Children, Yorkhill
Glasgow G3 8SJ (UK)
Tel. +44 141 201 0241, Fax +44 141 201 0837, E-Mail mdcd1t@clinmed.gla.ac.uk


 goto top of page Article Information

Received: October 16, 2006
Accepted: December 19, 2006
Published online: February 16, 2007
Number of Print Pages : 6
Number of Figures : 2, Number of Tables : 0, Number of References : 27

 
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Medline Abstract (ID 17308433)
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