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Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4496935

Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

About this item

Full title

Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

Publisher

England: BioMed Central Ltd

Journal title

Reproductive biology and endocrinology, 2015-07, Vol.13 (1), p.72-72, Article 72

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

49,XXXXY pentasomy or Fraccaro's syndrome is the most severe variant of Klinefelter's syndrome (KS) affecting about 1/85000 male births. The classical presentation is the triad: mental retardation, hypergonadotropic hypogonadism and radio ulnar synostosis. Indeed, the reproductive function of Fraccaro's syndrome is distinguished from KS. Besides, L...

Alternative Titles

Full title

Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4496935

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4496935

Other Identifiers

ISSN

1477-7827

E-ISSN

1477-7827

DOI

10.1186/s12958-015-0071-7

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