Dr

FEDERICA

DEODATO

Pediatric Neurologist in Division of Metabolism
Bambino Gesù Children's Hospital, Rome, Italy

About

DEODATO, FEDERICA

Dr. Federica Deodato is a Pediatric Neurologist in the Division of Metabolism at Bambino Gesù Children's Hospital in Rome, Italy. She specializes in neurometabolic disorders, with a focus on lysosomal storage diseases (LSDs), mucopolysaccharidoses (MPS), and metachromatic leukodystrophy (MLD). Her work contributes to advancing diagnostic accuracy, treatment strategies, and patient care for children affected by rare metabolic conditions.

Dr. Deodato is actively involved in clinical research, investigating innovative therapies for LSDs and other inherited metabolic disorders. She collaborates with international experts to improve early detection and intervention strategies, aiming to enhance long-term outcomes for pediatric patients. Her research includes studies on enzyme replacement therapy, gene therapy, and emerging treatment approaches that address the underlying causes of metabolic diseases.

Beyond her research, Dr. Deodato plays a key role in medical education and professional training, sharing her expertise with healthcare professionals and medical students. She participates in global initiatives focused on rare diseases, contributing to awareness campaigns and educational programs that promote early recognition and multidisciplinary management of neurometabolic disorders.

Her clinical work emphasizes early diagnosis and personalized treatment plans, ensuring that children with metabolic conditions receive comprehensive care tailored to their specific needs. She is dedicated to improving patient outcomes through multidisciplinary collaboration, working alongside geneticists, neurologists, and metabolic specialists to optimize therapeutic approaches.

Dr. Deodato has contributed to scientific publications and international conferences, presenting research findings that shape the future of pediatric metabolic medicine. Her commitment to advancing knowledge in the field continues to impact both clinical practice and research, fostering innovation in the diagnosis and treatment of rare diseases.

Appereances

Rare Diseases
Metachromatic Leukodystrophy
MLD
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