linear skin defects with multiple congenital anomalies 2 — Definition

Çoklu konjenital anomalilerle birlikte lineer cilt defektleri 2; linear skin defects with multiple congenital anomalies 2 is a rare genetic disease. This condition is characterized by linear (linear) skin scars or atrophic areas available in childbirth. It also accompanies congenital anomalies that affect multiple organs system such as heart, eye, skeleton and central nervous system. The disease is usually caused by a gene mutation that shows autozomal dominant inheritance.

The Turkish equivalent of "linear skin defects with multiple congenital anomalies 2" is Çoklu konjenital anomalilerle birlikte lineer cilt defektleri 2.

This term belongs to the Diseases category.