Yusuf S M, Mohammed A Z, Uloko A E
Dermatology Unit, Department of Medicine, Aminu Kano Teaching Kano, Nigeria.
Niger J Med. 2009 Oct-Dec;18(4):413-5. doi: 10.4314/njm.v18i4.51254.
Darier's disease is an autosomal dominant disorder characterized clinically by presence of keratotic papules in a seborrheic distribution, nail involvement and mucosal lesions. There are several clinical variants of Darier's disease, but few cases of segmental Darier's disease have been described in the literature. We describe a 12-year-old boy with type 2 mosaic phenotype. This unique clinical variant of Darier's disease has been described very rarely.
Darier病是一种常染色体显性疾病,临床特征为脂溢性分布的角化丘疹、指甲受累及黏膜损害。Darier病有多种临床变异型,但文献中报道的节段性Darier病病例较少。我们描述了一名患有2型嵌合表型的12岁男孩。Darier病的这种独特临床变异型极少被描述。