Conditions / Skin
autosomal recessive woolly hair 3
info · Skin
A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KRT24 gene on chromosome 17q21.2.
Signs and symptoms
- Curly hair
- Fine hair
- Sparse scalp hair
- Trichorrhexis nodosa
- Sparse eyelashes
- Sparse hair
Also known as: ARWH3