Chang Sing Pang A F, Oranje A P, Vuzevki V D, Stolz E
Arch Dermatol. 1981 Apr;117(4):225-8. doi: 10.1001/archderm.117.4.225.
Clinical features and treatment of keratoderma hereditaria mutilans (Vohwinkel's syndrome) are described in an 11-year-old boy. The disease, in particular the mutilating complications (pseudo-ainhum), responded satisfactorily to the oral administration of etretinate, an aromatic retinoid.
一名11岁男孩遗传性残毁性角化病(Vohwinkel综合征)的临床特征及治疗情况在此被描述。该疾病,尤其是残毁性并发症(假阿洪病),对芳香维甲酸依曲替酯的口服给药反应良好。