Maroua Garma

About the Author

Maroua Garma is a distinguished medical researcher and author specializing in rare genetic disorders, with a particular focus on the Gorlin-Goltz syndrome. Holding advanced degrees in genetics and clinical pathology, she has dedicated her career to unraveling the complexities of hereditary conditions that affect craniofacial and skeletal development. Her groundbreaking work bridges diagnostic challenges and clinical manifestations, offering invaluable insights for healthcare professionals worldwide. Through her meticulously researched publications, Garma advocates for early detection and multidisciplinary treatment approaches, emphasizing the human impact of these syndromes. Her contributions have been recognized in international medical forums, inspiring ongoing research and improved patient outcomes in the field of syndromology.