hypotrichosis 12

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2.

Signs and symptoms

• Dry hair
• Sparse scalp hair
• Sparse or absent eyelashes
• Sparse axillary hair
• Sparse pubic hair
• Aplasia/Hypoplasia of the eyebrow
• Slow-growing hair
• Abnormality of the dentition
• Abnormal nail morphology
• Abnormal sweat gland morphology

Also known as: HYPT12