Conditions / Genetic
spermatogenic failure 28
info ยท Genetic
A spermatogenic failure characterized by nonobstructive azoospermia and a Sertoli cell-only phenotype in testes that has_material_basis_in homozygous or compound heterozygous mutation in the FANCM gene on chromosome 14q21.2.
Signs and symptoms
- Male infertility
- Elevated circulating follicle stimulating hormone level
- Decreased testicular size
- Non-obstructive azoospermia
- Elevated circulating luteinizing hormone level
- Decreased serum testosterone concentration
Also known as: SPGF28