Two Males with SRY-Positive 46, XX Testicular Disorder of Sex Development

Date

2013

Authors

Gunes, S.
Asci, R.
Okten, G.
Atac, F.
Onat, O. E.
Ogur, G.
Aydin, O.
Ozcelik, T.
Bagci, H.

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Source Title

Systems Biology in Reproductive Medicine

Print ISSN

1939-6368

Electronic ISSN

1939-6376

Publisher

Taylor & Francis

Volume

59

Issue

1

Pages

42 - 47

Language

English

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Abstract

The 46,XX testicular disorder of sex development (46,XX testicular DSD) is a rare phenotype associated with disorder of the sex chromosomes. We describe the clinical, molecular, and cytogenetic findings of a 16-and a 30-year-old male patient with sex-determining region Y (SRY)-positive 46,XX testicular DSD. Chromosomal analysis revealed 46,XX karyotype. Fluorescence in situ hybridization (FISH) showed the SRY region translocated to the short arm of the X chromosome. The presence of the SRY gene was also confirmed by polymerase chain reaction (PCR). The X chromosome inactivation (XCI) assay showed that both patients have a random pattern of X chromosome inactivation. This report compares the symptoms and features of the SRY-positive 46,XX testicular DSD patients. © 2013 Informa Healthcare USA, Inc.

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Published Version (Please cite this version)