Overview
Anatalia Labilloy is a Medical Genetics provider in Boston, Massachusetts. Dr. Labilloy is rated as an Experienced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. Her top areas of expertise are Fabry Disease, Hypotonia, Mitochondrial Trifunctional Protein Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Dr. Labilloy is currently accepting new patients.
Her clinical research consists of co-authoring 14 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
The General Hospital Corporation
Amel Karaa is a Medical Genetics provider in Boston, Massachusetts. Dr. Karaa is rated as a Distinguished provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. Her top areas of expertise are MELAS Syndrome, Fabry Disease, Progressive External Ophthalmoplegia, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Karaa is currently accepting new patients.
C H Neurology Foundation Inc
Basil Darras is a Pediatric Neurologist and a Medical Genetics provider in Boston, Massachusetts. Dr. Darras is rated as an Elite provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. His top areas of expertise are Spinal Muscular Atrophy (SMA), Primary Lateral Sclerosis, Spinal Muscular Atrophy Type 2, Spinal Muscular Atrophy Type 1, and Gastrostomy. Dr. Darras is currently accepting new patients.
Massachusetts General Physicians Organization Inc
David Sweetser is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sweetser is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Trifunctional Protein Deficiency. His top areas of expertise are Hypotonia, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Propionic Acidemia. Dr. Sweetser is currently accepting new patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Fabry DiseaseDr. Labilloy isAdvanced. Learn about Fabry Disease.
- Experienced
- 2q37 Deletion SyndromeDr. Labilloy isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Labilloy isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Labilloy isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Labilloy isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Labilloy isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Labilloy isExperienced. Learn about Acrorenal Mandibular Syndrome.