Maheshwari Anshul, Dhaked Daulat Ram, Mathur Deepak K, Bhargava Puneet
Department of Dermatology, Venereology and Leprology, Sawai Man Singh Medical College, Jaipur, Rajasthan, India.
Indian Dermatol Online J. 2015 Sep-Oct;6(5):330-2. doi: 10.4103/2229-5178.164482.
Kindler syndrome (KS) is a very rare genodermatosis characterized by acral blistering starting in infancy along with photosensitivity, progressive poikiloderma, cutaneous atrophy, and a variable degree of mucosal involvement. A large number of other cutaneous and extracutaneous features have been described, which aid in diagnosing it. Generally KS has been found to be associated with hypohidrosis/anhidrosis. We herein present a rare case of KS with unique features.
金德勒综合征(KS)是一种非常罕见的遗传性皮肤病,其特征为婴儿期开始出现肢端水疱,伴有光敏性、进行性皮肤异色症、皮肤萎缩以及不同程度的黏膜受累。还描述了许多其他皮肤和皮肤外特征,有助于该病的诊断。一般发现KS与少汗症/无汗症有关。我们在此报告一例具有独特特征的罕见KS病例。