spermatogenic failure 35

A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 1

A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1.

Signs and symptoms

• Coiled sperm flagella
• Male infertility
• Absent sperm flagella
• Short sperm flagella
• Absent sperm axoneme central pair complex

Also known as: SPGF35