Conditions / Genetic
primary ovarian insufficiency 19
info · Genetic
A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22.
Signs and symptoms
- Premature ovarian insufficiency
- Secondary amenorrhea
- Irregular menstruation
- Female infertility
Also known as: POF19; POI19; premature ovarian failure 19