N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 Overview

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Learn About N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3

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However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

Who are the top N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 Local Doctors?
Laura A. Seth
Experienced in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
Internal Medicine
Experienced in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
Internal Medicine

Atrium Health Primary Care Charlotte Medical Clinic

3025 Springbank Lane, Suite 100, 
Charlotte, NC 
Experience:
34+ years
Languages Spoken:
English
Accepting New Patients
Offers Telehealth

Laura Seth is a primary care provider, practicing in Internal Medicine in Charlotte, North Carolina. Dr. Seth has been practicing medicine for over 34 years and is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. Her top areas of expertise are Hypothyroidism, Hyperthyroidism, Maturity Onset Diabetes of the Young, and Peripheral Neuropathy. Dr. Seth is currently accepting new patients.

Experienced in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
Experienced in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3

ETSU Physicians & Associates- Pediatrics

325 N State Of Franklin Rd, 
Johnson City, TN 
Languages Spoken:
English

. Dr. Russi is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His top areas of expertise are Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication.

 
 
 
 
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Robert W. Marion
Distinguished in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
Distinguished in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3

The Children's Hospital At Montefiore

3415 Bainbridge Avenue, 
Bronx, NY 
Languages Spoken:
English

Dr. Marion is Executive Director of the Children’s Evaluation and Rehabilitation Center and the University Center of Excellence in Developmental Disabilities at the Rose F. Kennedy Center. He is Chief of the Divisions of Genetics and of Development Medicine at the Children’s Hospital at Montefiore and Director of the Center for Congenital Disorders. A faculty member at Einstein since 1984, Dr. Marion’s interests include the natural history and genetic basis of multiple malformation syndromes. At The Children’s Hospital at Montefiore he has served as Medical Director of the Spina Bifida Center for 20 years, is the founder and Medical Director of the Williams Syndrome Center, and helped organize the Center for CardioG enetics, the Neurofibromatosis Center, and the Center for Excellence in Autism. He has published extensively in the medical literature in these areas and, in addition, is the author of seven books. Dr. Marion is rated as a Distinguished provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. His top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, and Mucopolysaccharidoses (MPS).

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