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[Genetics of male infertility]. / Genetik der männlichen Infertilität.
Tüttelmann, F; Gromoll, J; Kliesch, S.
Afiliação
  • Tüttelmann F; Institut für Humangenetik, Westfälische Wilhelms-Universität, Münster.
Urologe A ; 47(12): 1561-2, 1564-7, 2008 Dec.
Article em De | MEDLINE | ID: mdl-18953522
Genetic causes of male infertility increase in frequency with decreasing sperm concentration (oligo-/azoospermia). The decision about genetic tests should be made after a complete andrological work-up. Common causes comprise chromosomal aberrations (including Klinefelter syndrome), microdeletions of the AZF loci of the Y chromosome, mutations in the gene responsible for cystic fibrosis (CFTR) causing CBAVD and in genes involved in hypogonadotropic hypogonadism (including Kallmann syndrome). Every genetic investigation should be accompanied by comprehensive genetic counselling to help with the interpretation of results and support the patient/the couple concerning consequences for their family planning and treatment options.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azoospermia / Infertilidade Masculina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: De Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azoospermia / Infertilidade Masculina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: De Ano de publicação: 2008 Tipo de documento: Article