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Pachyonychia Congenita Type 2 -A Case Report-

Fu‐Sen Hsieh、J. Yu-Yun Lee、Sheau‐Chiou Chao

2001Biochemistry, Genetics and Molecular Biology被引 1

摘要

Pachyonychia congenital type2 (PC-2), also known as Jackson-Lawler type PC, is a rare autosomal dominant disorder characterized by hypertrophic nail dystrophy associated with focal palmoplantar keratoderma and multiple pilosebceous cysts. Only one case of PC-1 has been previously reported in Taiwan. In this report, we describe a typical case of PC-2, the first such case to be documented in Taiwan. The keratoderma was treated with etretinate, which was quite effective in reducing the hyperkeratotic lesions on the patient’s palms and soles.

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DOI：https://doi.org/10.29784/ds.200109.0004