spermatogenic failure 11

A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21.

Signs and symptoms

• Male infertility
• Oligozoospermia
• Abnormal sperm morphology
• Reduced sperm motility

Also known as: SPGF11