Articles Related to genetic disorder
Parry Romberg Syndrome: A Case Report
Parry-Romberg syndrome is a rare disorder characterized by slowly progressive deterioration of the skin and soft tissues of half of the face. The syndrome presents with characteristic skeletal, dental, and soft tissue changes in the affected half of the face, with or without neurological signs and symptoms.
Editorial Board Members Related to genetic disorder
Huda Faleh Gharaibeh
Associate Professor
Maternal Child Health Department
Faculty of Nursing
Jordan University of Science and Technology
Jordan
Maternal Child Health Department
Faculty of Nursing
Jordan University of Science and Technology
Jordan