Autosomal recessive cutis laxa type-1 with complex systemic manifestations

• 主要な著者: Shruti Dhanraj Chavan (著者), Ashish Ramchandra Deshmukh (著者), Aniruddha Dharnidhar Gulanikar (著者), Shilpa Satyajeet Pathrikar (著者), Iqbal Mohammad Tariq (著者)
• フォーマット: 図書
• 出版事項: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Cutis laxa (CL) is a rare connective tissue disorder characterized by loose, sagging, and redundant skin. Both inherited and acquired forms are known. A 7-year-old boy, presented with loose, sagging skin chiefly over the face, extremities, and skin folds since birth with recurrent respiratory and sy...