Autosomal recessive cutis laxa type-1 with complex systemic manifestations

• Main Authors: Shruti Dhanraj Chavan (Author), Ashish Ramchandra Deshmukh (Author), Aniruddha Dharnidhar Gulanikar (Author), Shilpa Satyajeet Pathrikar (Author), Iqbal Mohammad Tariq (Author)
• Format: Book
• Published: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
• Subjects: article
• Online Access: 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...