MediFind found 10 doctor with experience in N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 near Michigan, US. Of these, 10 are Experienced.
Regents Of The University Of Michigan
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ahmad 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 Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Classic Galactosemia. Dr. Ahmad is currently accepting new patients.
Regents Of The University Of Michigan
Elizabeth Ames is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ames 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 Delayed Growth, Cardiomyopathic Lentiginosis, Noonan Syndrome, and Cardiofaciocutaneous Syndrome. Dr. Ames is currently accepting new patients.
Regents Of The University Of Michigan
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Quinonez 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 Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Propionic Acidemia.
Spectrum Health Primary Care Partners
Benjamin Schipper is a primary care provider, practicing in Pediatrics and Internal Medicine in Grand Rapids, Michigan. Dr. Schipper 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 Obesity in Children, Food Allergy, Down Syndrome, and Hashimoto Thyroiditis. Dr. Schipper is currently accepting new patients.
Regents Of The University Of Michigan
Christina Sloan is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Sloan 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 Chromosome 8p Deletion, Chromosome 6q Duplication, Delayed Growth, and Fragile XE Syndrome.
Regents Of The University Of Michigan
Tomoyasu Higashimoto is a Medical Genetics provider in Ann Arbor, Michigan. Dr. Higashimoto 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 Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia.
Regents Of The University Of Michigan
Mark Hannibal is a Pediatrics specialist and a Medical Genetics provider in Ann Arbor, Michigan. Dr. Hannibal 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 Aase Syndrome, Filippi Syndrome, CHARGE Syndrome, and Smith-Kingsmore Syndrome.
Spectrum Health Primary Care Partners
Jessica Priestley is a Medical Genetics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Priestley 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 Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is currently accepting new patients.
Regents Of The University Of Michigan
Amanda Pritchard is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Pritchard 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 Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Aase Syndrome.
Regents Of The University Of Michigan
Kristen Lee is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Lee 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 Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome.
Last Updated: 10/30/2025