De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia
Author(s) -
Ioannis Papoulidis,
Annalisa Vetro,
Konstantinos Kefalas,
Sandro Orrù,
Loretta Thomaidis,
Zoi Iliodromiti,
Orsetta Zuffardi,
Emmanouil Manolakos
Publication year - 2013
Publication title -
molecular syndromology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 36
eISSN - 1661-8777
pISSN - 1661-8769
DOI - 10.1159/000351656
Subject(s) - phenotype , genetics , comparative genomic hybridization , oligospermia , gene , chromosome , biology , azoospermia , infertility , pregnancy
We describe a case of a 34-year-old male presenting with oligospermia and an otherwise normal phenotype. Investigation with array-based comparative genomic hybridization (aCGH) revealed an interstitial deletion of about 15.5 Mb in chromosome 5p13.3p14.3. We compared the phenotype of our patient with recently reported patients studied by aCGH, who show an overlapping deletion. We also analyzed the gene content of the deleted region in order to propose a possible involvement of specific genes in the clinical phenotype.
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