Piletta P A, Calza A M, Masouyé I, Harms M, Saurat J H
Clinique de Dermatologie et Vénéréologie, Hôpital Cantonal Universitaire de Genève, Suisse.
Dermatology. 1995;191(4):355-8. doi: 10.1159/000246601.
An isolated affected 19-year-old male with hypohidrotic ectodermal dysplasia (HED) had rare features of the syndrome such as recurrent otitis and multiple sebaceous gland papules of the face. Sebaceous gland hypertrophy is puzzling in the context of HED.
一名患有少汗型外胚层发育不良（HED）的19岁孤立性患病男性具有该综合征的罕见特征，如复发性中耳炎和面部多发性皮脂腺丘疹。在HED的背景下，皮脂腺肥大令人费解。
