The 20 Best N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3 Doctors Near Me in Michigan, US

Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Von Gierke Disease, and Tyrosinemia Type 3. Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Ahmad is currently accepting new patients.

Elizabeth Ames is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Noonan Syndrome, Cardiofaciocutaneous Syndrome, and Cardiomyopathic Lentiginosis. Dr. Ames is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics & Genomics. Dr. Ames is currently accepting new patients.

Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. He is also highly rated in 129 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Maple Syrup Urine Disease. Dr. Quinonez is board certified in Pediatrics, American Board Of Pediatrics, Pediatrics - 2011, Clinical Biochemical Genetics, American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2015 , American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2024 , and Clinical Genetics & Genomics. Dr. Quinonez is currently accepting new patients.

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. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Obesity in Children, Food Allergy, Down Syndrome, and Hashimoto Thyroiditis. Dr. Schipper is board certified in American Board Of Internal Medicine and American Board Of Pediatrics. Dr. Schipper is currently accepting new patients.

Tomoyasu Higashimoto is a Medical Genetics provider practicing medicine 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. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics. Dr. Higashimoto is currently accepting new patients.

Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. He is also highly rated in 167 other conditions, according to our data. His clinical expertise encompasses Aase Syndrome, Alstrom Syndrome, Char Syndrome, and Filippi Syndrome. Dr. Hannibal is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2020 and Clinical Genetics & Genomics. Dr. Hannibal is currently accepting new patients.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Priestley is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics. Dr. Priestley is currently accepting new patients.

Amanda Pritchard is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 150 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant. Dr. Pritchard is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2019 , American Board Of Pediatrics, Pediatrics - 2016, and American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2019 . Dr. Pritchard is currently accepting new patients.

Kristen Lee is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 138 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome. Dr. Lee is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics & Genomics. Dr. Lee is currently accepting new patients.

Esperanza Font-Montgomery is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Detroit, Michigan. Dr. Font-Montgomery is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, Pompe Disease, Danon Disease, and Phenylketonuria (PKU). Dr. Font-Montgomery is currently accepting new patients.

Christina Sloan-Heggen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Sloan-Heggen is rated as an Experienced provider by MediFind in the treatment of N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Duplication, Chromosome 8p Deletion, Delayed Growth, and Fragile XE Syndrome. Dr. Sloan-Heggen is board certified in Medical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Sloan-Heggen is currently accepting new patients.