Literature DB >> 891369

[Primary amenorrhoea, hypertension, and hypokalaemia in 17-hydroxylase deficiency, a not uncommon condition (author's transl)].

W E de Lange, R E Lappöhn, W J Sluiter, H Doorenbos.   

Abstract

Five phenotypic female patients with primary amenorrhoea, mild hypertension, and hypokalaemia are described. The condition originates from 17-hydroxylase deficiency in both adrenals and gonads. Two cases had a XY chromosome pattern, two cases were familial. It is suggested to determine serum potassium in all cases with unexplained primary amenorrhoea.

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Year:  1977        PMID: 891369     DOI: 10.1055/s-0028-1105458

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  3 in total

1.  Male pseudohermaphroditism due to 17-hydroxylase deficiency.

Authors:  A D'Alberton; E Reschini; T Motta; A Catania
Journal:  J Endocrinol Invest       Date:  1989-03       Impact factor: 4.256

2.  Spontaneous sexual development and menarche in a female with 17 alpha-hydroxylase deficiency.

Authors:  P N Singhellakis; D Panidis; J Papadimas; H Demertzi; A Tsourdis; F Sotsiou; D G Ikkos
Journal:  J Endocrinol Invest       Date:  1986-04       Impact factor: 4.256

3.  Male pseudohermaphroditism: genetics and clinical delineation.

Authors:  J L Simpson
Journal:  Hum Genet       Date:  1978-10-19       Impact factor: 4.132

  3 in total

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