Fertility and sterility · 2001
Chromosomal translocation 3;22 in an infertile man.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Quintana de la Rosa J L, Gallegos Avila G, García Cavazos R, Zungri Telo E
Аннотация
OBJECTIVE: To present the first case of an infertile male with a normal phenotype and chromosomal translocation 3;22.
DESIGN: Case report.
SETTING: POVISA Medical Center.
PATIENT(S): A 45-year-old man with primary infertility for 13 years and with different partners; the patient has a family history of recurrent miscarriages and low fertility.
INTERVENTION(S): Lymphocytic karyotype and electron microscopy.
MAIN OUTCOME MEASURE(S): Physical examination and semen analysis.
RESULT(S): The semen analysis revealed oligoasthenoteratospermia. The lymphocytic karyotype detected a translocation 3;22, and electron microscopy showed a lack of the central microtubule pair and peripheral doublet.
CONCLUSION(S): An association between translocation 3;22 and other abnormalities in infertile males has been reported, but no such association has ever been described in men whose only clinical manifestation is infertility.
DESIGN: Case report.
SETTING: POVISA Medical Center.
PATIENT(S): A 45-year-old man with primary infertility for 13 years and with different partners; the patient has a family history of recurrent miscarriages and low fertility.
INTERVENTION(S): Lymphocytic karyotype and electron microscopy.
MAIN OUTCOME MEASURE(S): Physical examination and semen analysis.
RESULT(S): The semen analysis revealed oligoasthenoteratospermia. The lymphocytic karyotype detected a translocation 3;22, and electron microscopy showed a lack of the central microtubule pair and peripheral doublet.
CONCLUSION(S): An association between translocation 3;22 and other abnormalities in infertile males has been reported, but no such association has ever been described in men whose only clinical manifestation is infertility.