Conditions / Genetic
primary pigmented nodular adrenocortical disease 2
info · Genetic
A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2.
Signs and symptoms
- Pigmented micronodular adrenocortical disease
- Increased circulating cortisol level
- Osteoporosis
- Depression
- Osteopenia
- Anxiety
- Emotional lability
- Bruising susceptibility
- Agitation
- Round face
Also known as: PPNAD2