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Details

Autor(en) / Beteiligte
Titel
Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men
Ist Teil von
  • Brazilian journal of medical and biological research, 2006-04, Vol.39 (4), p.555-561
Ort / Verlag
Brazil: Associação Brasileira de Divulgação Científica
Erscheinungsjahr
2006
Link zum Volltext
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • The objective of the present study was to determine the frequency of somatic chromosomal anomalies and Y chromosomal microdeletions (azoospermia factor genes, AZF) in infertile males who seek assisted reproduction. These studies are very important because the assisted reproduction techniques (mainly intracytoplasmic sperm injection) bypass the natural selection process and some classical chromosomal abnormalities, microdeletions of AZF genes or some deleterious genic mutations could pass through generations. These genetic abnormalities can cause in the offspring of these patients male infertility, ambiguous external genitalia, mental retardation, and other birth defects. We studied 165 infertile men whose infertility was attributable to testicular problems (60 were azoospermic, 100 were oligospermic and 5 were asthenospermic). We studied 100 metaphases per patient with GTG banding obtained from temporary lymphocyte culture for chromosomal abnormality detection and performed a genomic DNA analysis using 28 Y chromosome-specific sequence-tagged sites for Y AZF microdeletion detection. Karyotyping revealed somatic anomalies in 16 subjects (16/165 = 9.6%). Of these 16, 12 were in the azoospermic group (12/60 = 20%) and 4 were in the oligospermic group (4/100 = 4%). The most common chromosomal anomaly was Klinefelter syndrome (10/165 = 6%). Microdeletions of AZF genes were detected in 12 subjects (12/160 = 7.5%). The frequencies detected are similar to those described previously. These results show the importance of genetic evaluation of infertile males prior to assisted reproduction. Such evaluation can lead to genetic counseling and, consequently, to primary and secondary prevention of mental retardation and birth defects.
Sprache
Englisch; Portugiesisch
Identifikatoren
ISSN: 0100-879X, 1414-431X
eISSN: 1414-431X
DOI: 10.1590/S0100-879X2006000400017
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_e03d2831f3de4a93b21a8780b1d331ab

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