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Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency

Clinical Endocrinology

Jan 1, 1976

J TourniaireMaguelone G Forest

PMID: 174842

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Abstract

A case of male pseudohermaphroditism aged 48 years with systemic hypertension and hypokalaemic alkalosis is described. Results of metabolic studies point to a 17alpha-hydroxylase deficiency demonstrated by low cortisol (0-56 mg/24 h), high corticosterone (270 mg/24 h) and 11-deoxycortic...read more

Mentioned in this Paper

Cell Secretion
Metabolic Abnormality Assessment
Estrone
Intersexuality
Corticotropin
Alkalosis
Hypokalemic Alkalosis
Renin Measurement
Radionuclide Metabolic Studies
Disorders of Sex Development
Paper Details
References
  • References9
  • Citations12
12

Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency

Clinical Endocrinology

Jan 1, 1976

J TourniaireMaguelone G Forest

PMID: 174842

DOI:

Abstract

A case of male pseudohermaphroditism aged 48 years with systemic hypertension and hypokalaemic alkalosis is described. Results of metabolic studies point to a 17alpha-hydroxylase deficiency demonstrated by low cortisol (0-56 mg/24 h), high corticosterone (270 mg/24 h) and 11-deoxycortic...read more

Mentioned in this Paper

Cell Secretion
Metabolic Abnormality Assessment
Estrone
Intersexuality
Corticotropin

Related Papers

Paper Details
References
  • References9
  • Citations12
12

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