Acropigmentation of Kitamura with immigration delay disease: A rare entity

• المؤلفون الرئيسيون: Sumir Kumar (مؤلف), Bharat Bhushan Mahajan (مؤلف), Nidhi Kamra (مؤلف), Pritish A Bhoyar (مؤلف)
• التنسيق: كتاب
• منشور في: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Reticulate acropigmentation of Kitamura (RAK) is a rare, autosomal dominant disorder first described in Japan characterised by a reticulate pattern of slightly atrophic, angulated, hyperpigmented macules affecting the acral areas of the body. We hereby report a case of RAK in a young Indian male wit...