Literature DB >> 989221

A case of male pseudohermaphroditism associated with elevated LH, normal FSH and low testosterone possibly due to the secretion of an abnormal LH molecule.

I J Park, L S Burnett, H W Jones, C J Migeon, R M Blizzard.   

Abstract

A 27 year old female is described who had 46,XY chromosome complement, ambiguous external genitalia with elevated LH, slightly above normal FSH and low testosterone. Her plasma testosterone level increased 15-20 fold after HCG stimulation (5000 IU X 3). then returned to prestimulation level 3 months later. This was possibly due to the secretion of an abnormal LH molecule which is immunoreactive but biologically inactive in the human.

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Year:  1976        PMID: 989221     DOI: 10.1530/acta.0.0830173

Source DB:  PubMed          Journal:  Acta Endocrinol (Copenh)        ISSN: 0001-5598


  2 in total

1.  Male pseudohermaphroditism secondary to panhypopituitarism.

Authors:  D P Burgner; S Kinmond; A M Wallace; D G Young; M G Forest; M D Donaldson
Journal:  Arch Dis Child       Date:  1996-08       Impact factor: 3.791

2.  Male pseudohermaphroditism: genetics and clinical delineation.

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

  2 in total

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