Abstract
Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16, or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy. Available studies assessing oral retinoid treatment for PC are limited to a few case reports.
| Original language | English |
|---|---|
| Pages (from-to) | e193-9 |
| Journal | Journal of the American Academy of Dermatology |
| Volume | 66 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2012 |
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