Document Detail


Male pseudohermaphroditism due to partial end-organ insensitivity to androgens.
MedLine Citation:
PMID:  890997     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A 46XY individual with incomplete male pseudohermaphroditism was studied. The phenotype was distinctive, with a masculine habitus despite a small phallus, gynaecomastia and diminished virilization. Plasma levels of testosterone, oestrogens, gonadotrophins and sex-hormone binding globulin were elevated. It is proposed that this syndrome is a variant of Type I incomplete male pseudohermaphroditism.
Authors:
J M Barragry; H L Makin; D V Morris; D J Trafford; A S Mason
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Clinical endocrinology     Volume:  7     ISSN:  0300-0664     ISO Abbreviation:  Clin. Endocrinol. (Oxf)     Publication Date:  1977 Aug 
Date Detail:
Created Date:  1977-10-28     Completed Date:  1977-10-28     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0346653     Medline TA:  Clin Endocrinol (Oxf)     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  137-41     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adult
Gonadal Steroid Hormones / blood
Gonadotropins, Pituitary / blood
Humans
Male
Phenotype
Pseudohermaphroditism / blood,  etiology*
Receptors, Androgen*
Receptors, Steroid*
Chemical
Reg. No./Substance:
0/Gonadal Steroid Hormones; 0/Gonadotropins, Pituitary; 0/Receptors, Androgen; 0/Receptors, Steroid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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