Conditions / Syndrome
dermatopathia pigmentosa reticularis
info · Syndrome
An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in the KRT14 gene on chromosome 17q21.2.
Signs and symptoms
- Alopecia of scalp
- Abnormal conjunctiva morphology
- Adermatoglyphia
- Reticular hyperpigmentation
- Hypohidrosis
- Palmoplantar hyperkeratosis
- Nail dystrophy
- Reticulate pigmentation of oral mucosa
Also known as: DPR