Conditions / Skin
hypotrichosis 1
info · Skin
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the APCDD1 gene on chromosome 18p11.22.
Signs and symptoms
- Sparse hair
- Sparse body hair
- Sparse pubic hair
- Sparse axillary hair
- Abnormality of the dentition
- Abnormal nail morphology
- Sparse eyelashes
- Sparse eyebrow
- Abnormality of the skin
Also known as: HHS; HTS; HYPT1; hereditary generalized hypotrichosis simplex