Rosenthal Syndrome

Rosenthal Syndrome is a rare genetic condition characterized by a combination of features, including a specific type of hair loss, skin abnormalities, and sometimes neurological or developmental issues. People with this syndrome may have sparse or absent hair, particularly on the scalp and other parts of the body. The condition can also involve other physical anomalies, such as facial differences. It results from a genetic mutation and is typically diagnosed through clinical evaluation. Management focuses on addressing the individual symptoms and providing support tailored to the person’s needs.