克罗斯顿综合征：一名患者的25年随访

Trídico Lívia Arroyo, Antonio João Roberto, Pozetti Eurides Maria de Oliveira, Rosa Ana Maria Mendes, Antonio Carlos Roberto

Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto, SP, Brazil.

An Bras Dermatol. 2015 Nov-Dec;90(6):897-9. doi: 10.1590/abd1806-4841.20153990.

Clouston syndrome is a rare genodermatosis that affects skin and annexes. It is a form of ectodermal dysplasia characterized by generalized hypotrichosis, palmoplantar hyperkeratosis and nail dystrophy. This paper reports a 25-year follow-up of a patient with Clouston syndrome, from childhood to adulthood, monitoring diagnosis and clinical course of the disease.

克罗斯顿综合征是一种罕见的影响皮肤及其附属器的遗传性皮肤病。它是外胚层发育不良的一种形式，其特征为全身性毛发稀少、掌跖角化过度和甲营养不良。本文报告了一名克罗斯顿综合征患者从儿童期到成年期的25年随访情况，监测了该疾病的诊断和临床病程。