The 20 Best Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome) 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 a Distinguished provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.

Dr. Meisner is a board-certified pediatric cardiologist and physician scientist. His clinical focus is on cardiovascular genetics, and he provides the pediatric cardiology services in the multidisciplinary hypertrophic cardiomyopathy, muscular dystrophy, cardiovascular genetics and aortopathy, and RASopathy clinics. He also sees general cardiology and molecular and biochemical cardiology patients in his individual clinics. His translational research laboratory utilizes induced pluripotent stem cell cardiomyocyte and innovative mouse models to understand the pathophysiology and clinical course that leads to cardiomyopathy in children and young adults. Dr. Meisner is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 23 other conditions, according to our data. His clinical expertise encompasses CHARGE Syndrome, Noonan Syndrome, Cardiomyopathic Lentiginosis, and Cardiofaciocutaneous Syndrome. Dr. Meisner is board certified in Pediatric Cardiology and Pediatrics.

Thor Thorsson is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Thorsson is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 107 other conditions, according to our data. His clinical expertise encompasses Tetralogy of Fallot, Hypoplastic Left Heart Syndrome (HLHS), Mitral Atresia, and Isthmian Coarctation. Dr. Thorsson is board certified in Pediatric Cardiology.

Albert Rocchini is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Rocchini is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Hypoplastic Left Heart Syndrome (HLHS), Tetralogy of Fallot, Ventricular Septal Defects, Patent Foramen Ovale Repair, and Stent Placement.

Brooke Geddie is a Pediatrics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 21 years. Dr. Geddie is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 47 other conditions, according to our data. Her clinical expertise encompasses Coloboma, Strabismus, Congenital Cataract, Esotropia, and Vitrectomy. Dr. Geddie is board certified in American Osteopathic Board Of Ophthalmology & Otolaryngology.

Patrick Droste is a Pediatrics provider practicing medicine in Grand Rapids, Michigan. He has been practicing medicine for over 46 years. Dr. Droste is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 35 other conditions, according to our data. His clinical expertise encompasses Strabismus, Esotropia, Amblyopia, and Brown Syndrome. Dr. Droste is board certified in American Board Of Ophthalmology. Dr. Droste is currently accepting new patients.

Jimmy Lu is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Lu is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 129 other conditions, according to our data. His clinical expertise encompasses Tetralogy of Fallot, Hypoplastic Left Heart Syndrome (HLHS), Double Discordia, Transposition of the Great Arteries, and Heart Transplant. Dr. Lu is board certified in Pediatric Cardiology.

Jeffrey Cassidy is a Pediatric Orthopedics provider practicing medicine in Grand Rapids, Michigan. He has been practicing medicine for over 29 years. Dr. Cassidy is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Scoliosis, Caudal Regression Syndrome, Spondylocarpotarsal Synostosis Syndrome, Osteotomy, and Spinal Fusion. Dr. Cassidy is board certified in American Board Of Orthopaedic Surgery. Dr. Cassidy is currently accepting new patients.

Dr. Pasquali is the Janette Ferrantino Professor of Pediatrics and the Interim Associate Chief Clinical Officer for C.S. Mott Children’s Hospital at the University of Michigan. She has previously served as the Service Chief for the Division of Pediatric Cardiology and the Director of Research and Quality within the Congenital Heart Center. Dr. Pasquali received her undergraduate degree from University of Michigan and medical degree from Duke University School of Medicine. She completed pediatric residency and pediatric cardiology fellowship training at the Children’s Hospital of Philadelphia. She has a Masters of Health Sciences degree in Clinical Research, and has completed executive leadership training through the ELAM program.Dr. Pasquali’s work has focused on optimizing pediatric care and outcomes both locally and across the country through research, quality, and policy efforts. She has authored more than 200 publications in this area and her research has been continuously funded by the NIH throughout her career. She is the Co-PI for her center’s participation as one of 9 core sites in NHLBI-funded Pediatric Heart Network, and was a co-founder of Cardiac Networks United which has fostered collaboration spanning more than two thirds of the nation’s congenital heart programs to support novel research and quality efforts that have improved care and outcomes across children’s hospitals. She recently led an initiative that brought together 15 professional societies and 20+ institutions to develop the first multi-disciplinary consensus guidelines for congenital heart surgery in the US. Dr. Pasquali is the immediate past chair of the American Heart Association Scientific Sessions for the Young Hearts Council, and is an active mentor, recently launching a national early career exchange program across congenital heart centers.Dr. Pasquali has received numerous awards including the Outstanding Research Award in Pediatric Cardiology from the American Heart Association, and Richard E. Clark Award from the Society of Thoracic Surgeons. Dr. Pasquali is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Hypoplastic Left Heart Syndrome (HLHS), Coarctation of the Aorta, Tetralogy of Fallot, Heart Transplant, and Aortic Valve Replacement. Dr. Pasquali is board certified in Pediatric Cardiology.

Sarah Gelehrter is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Gelehrter is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Hypoplastic Left Heart Syndrome (HLHS), Tetralogy of Fallot, Mitral Atresia, Lithotripsy, and Gastrostomy. Dr. Gelehrter is board certified in Pediatric Cardiology.

Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). 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, Clinical Biochemical Genetics, and Clinical Genetics & Genomics.

Andrea Amalfitano is a Medical Genetics provider practicing medicine in Okemos, Michigan. Dr. Amalfitano is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Pompe Disease, and Balloon Sinuplasty.

Joseph Nettleman is a primary care provider, practicing in Family Medicine in Lansing, Michigan. Dr. Nettleman is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Cerebral Palsy, and Selective Deficiency of IgA.

Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency. Dr. Adams is currently accepting new patients.

Dr. DeGuzman is a graduate of the University of Michigan Medical School. He completed his residency training in Internal Medicine and additionally served as Chief Medical Resident at the University of Michigan Hospitals. Dr. DeGuzman has been closely involved in medical education. He is a member of the Doctoring Course Faculty, teaching both preclinical and clinical medical students in small group and individual settings. Additionally, he mentors resident physicians in Primary Care General Medicine clinic. He is an avid runner and triathlete and enjoys spending time with his wife and three children. Dr. Deguzman is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Glucocorticoid-Remediable Aldosteronism, Hypertension, Familial Hypertension, and Type 2 Diabetes (T2D).

Dr. Shahzad Mian serves as Chair and professor in the Department of Ophthalmology and Visual Sciences at the University of Michigan Medical School and has served the department as vice chair for clinical sciences and learning since 2019. He also serves as the ambulatory care clinical chief for the University of Michigan Medical Group (UMMG).Dr. Mian earned his medical degree in 1996 from the Emory University School of Medicine. He then completed a residency at the Wills Eye Hospital of Thomas Jefferson University in Philadelphia. From 2000-02, he was a fellow in cornea and refractive surgery at Harvard Medical School, Massachusetts Eye and Ear Infirmary. He joined the U-M faculty in 2002 as a clinical lecturer in ophthalmology and visual sciences, and he was promoted to associate professor of ophthalmology and visual sciences in 2010.Dr. Mian received the 2007 Anthony Adamis Award for Outstanding Research from the U-M Kellogg Eye Center, the 2007 Leadership Development Program from the American Academy of Ophthalmology and the 2009 Achievement Award from the American Academy of Ophthalmology.He has served on the board of directors and as a medical director of the Midwest Eye-Banks and currently serves as cornea editor for the Ophthalmic News and Education Network, board member of the Cornea Society, member of the Program Director’s Council and councilor for the American Academy of Ophthalmology. Dr. Mian is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 42 other conditions, according to our data. His clinical expertise encompasses Cataract, Interstitial Keratitis, Fuchs Dystrophy, Corneal Transplant, and Cataract Removal. Dr. Mian is board certified in Ophthalmology.

Cooking, spending time with my family. Dr. Ames is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Cardiomyopathic Lentiginosis, Cardiofaciocutaneous Syndrome, and Noonan Syndrome. Dr. Ames is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.

Dr. Jacobson completed residency in New York and a fellowship in pediatricophthalmology at the Kellogg Eye Center. His interests include medicaleducation and pediatric glaucoma. He is currently one of the associatemedical student clerkship directors and manages patients with pediatricglaucoma at the University of Michigan. Dr. Jacobson is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). He is also highly rated in 43 other conditions, according to our data. His clinical expertise encompasses Stickler Syndrome, Axenfeld-Rieger Syndrome, Microphthalmia, Trabeculectomy, and Vitrectomy. Dr. Jacobson is board certified in Ophthalmology.

Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). 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. Keefer works on the Pediatric Hospitalist, Pediatric Palliative Care, and Adult Palliative Care services and has a special interest in improving quality of life for chronically ill children and treating pain in terminal illness. Dr. Keefer is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Trisomy 13, CHARGE Syndrome, Early Infantile Epileptic Encephalopathy, and Wildervanck Syndrome. Dr. Keefer is board certified in Internal Medicine, Pediatrics, and Hospice & Palliative Med.