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Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma
1Department of Dermatology, Worthing Hospital, Western Hospitals NHS Trust, Worthing, West Sussex, UK.
Punctate palmoplantar keratoderma type 1 (PPPK1), a rare inherited skin condition, is caused by mutations in the AAGAB gene. This study identifies three recurrent mutations in AAGAB linked to PPPK1 in affected families.
Area of Science:
- Dermatology
- Genetics
- Molecular Biology
Background:
- Punctate palmoplantar keratoderma type 1 (PPPK1) is a rare autosomal dominant inherited skin disorder.
- It is characterized by hyperkeratotic lesions on palms and soles.
- The AAGAB gene, encoding p34 protein, has been identified as the causative gene for PPPK1.
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