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PMID 12801575
Gene Name DAZ1
Condition Infertility
Association The results of this study indicate that reduced copy number of DAZ genes may not necessarily lead to infertility. Partial deletions od DAZ gene were also found to be transmitted from one genration to the next
Mutation Reduced copy number of the DAZ genes
Population size 9
Population details 5 siblings (primary infertility),
Age Patient age: 38, Pateients fathers age: 64
Sex Male
Infertility type Male infertility
Other associated phenotypes Azoospermia, Oligozoospermia


Partial DAZ deletions in a family with five infertile brothers

Gianotten J, Hoffer MJ, De Vries JW, Leschot NJ, Gerris J, van der Veen F.

OBJECTIVE: To study the genetic cause of infertility in a family with five infertile brothers. DESIGN: Case report. SETTINGS: Center for reproductive medicine at a university medical center. PATIENT(S): Five brothers presenting with primary infertility due to severely impaired spermatogenesis; also, their parents and two other paternally related family members. INTERVENTION(S): Fluorescence in situ hybridization and sequence family variant analysis was performed in leukocyte DNA to determine the number of deleted in azoospermia (DAZ) genes. Linkage analysis was performed for X chromosome inheritance, and mitochondrial DNA (mtDNA) was screened for mutations. MAIN OUTCOME MEASURE(S): DAZ gene copy number, X chromosome linkage, and mtDNA sequence. RESULT(S): With conventional polymerase chain reaction (PCR) analysis, no deletions of the AZFc region were found, but with fluorescence in situ hybridization and sequence family variant analysis, only two DAZ genes instead of four were detected in all individuals tested. The five brothers did not share an identical X chromosomal locus, and no mutations were found in the mtDNA of the index patient. CONCLUSION(S): A reduced copy number of the DAZ genes is found in five infertile brothers with severely impaired spermatogenesis, as well as in their normospermic father and in two other fertile paternally related family members. This illustrates that the phenotype associated with a reduced copy number of the DAZ genes can be extremely variable. FAU - Gianotten, Judith AU - Gianotten J AD - Center for Reproductive Medicine, Academic Medical Center, The, Amsterdam, Netherlands. j.gianotten@amc.uva.nl FAU - Hoffer, Mariƫtte J V AU - Hoffer MJ FAU - De Vries, Jan W A AU - De Vries JW FAU - Leschot, Nico J AU - Leschot NJ FAU - Gerris, Jan AU - Gerris J