Transmission of de novo mutations of the deleted in azoospermia genes from a severely oligozoospermic male to a son via intracytoplasmic sperm injection

Objective: To investigate the transmission of microdeletions in the deleted in azoospermia ( DAZ) genes to a male offspring via intracytoplasmic sperm injection (ICSI). Design: Case report. Setting: Reproductive unit of a university teaching hospital. Patient(s): A 29-year-old, severely oligozoospermic male with microdeletions of the DAZ genes in Yq interval 6 and his son, who was conceived via ICSI. Intervention(s): DNA screening for the microdeletions in Yq interval 6 with 24 sequence tagged sites with the use of polymerase chain reaction amplification for the patient, the patient’s father, and the patient’s son. Paternity identification was performed using nine hypervariable short tandem repeats. Main Outcome Measure(s): Deletion mapping of Yq interval 6 from sequence tagged sites and electropherogram of short tandem repeats for DNA fingerprinting. Result(s): The son had the same microdeletions of the DAZ genes as the patient, and the patient’s father had normal DAZ genes. The paternity of the patient, the patient’s father, and the patient’s son was verified. Conclusion(s): De novo DAZ microdeletions in an infertile male can be transmitted to a male offspring via ICSI. DNA screening tests for DAZ genes before ICSI may help in the genetic counseling of patients with idiopathic azoospermia or severe oligozoospermia.