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