H Husseini

Autosomal Dominant Cutis Laxa type 3 in a Lebanese female child: a case report and literature review about an exceptionally rare genetic disease

Abstract Cutis Laxa is a heterogeneous group of diseases characterized by a loose, wrinkled and prematurely aged skin appearance and have been documented to be transmitted through autosomal recessive, autosomal dominant, or X-linked patterns. With an estimated prevalence of less...