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    Last Updated: 01/09/2026

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    MediFind found 19 doctor with experience in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) near Michigan, US. Of these, 16 are Experienced and 3 are Advanced.

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    19 providers found
      John W. Kemppainen
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Orthopedics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Orthopedics

      Corewell Health Pediatric Orthopedics - 35 Michigan St NE

      35 Michigan Street Northeast, Suite 4150, 
      Grand Rapids, MI 
      Experience:
      19+ years
      Languages Spoken:
      English
      Accepting New Patients

      John Kemppainen is a Pediatric Orthopedics provider in Grand Rapids, Michigan. Dr. Kemppainen has been practicing medicine for over 19 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Clubfoot, Legg-Calve-Perthes Disease (LCPD), Knock Knees, and Small Patella Syndrome. Dr. Kemppainen is currently accepting new patients.

      Jessica R. Priestley
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Medical Genetics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Medical Genetics

      Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE

      25 Michigan Street Northeast, Suite 2100, 
      Grand Rapids, MI 
      Experience:
      8+ years
      Languages Spoken:
      English

      Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.

      Marian M. Bercu
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      General Surgery
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      General Surgery

      Corewell Health Pediatric Neurosurgery - 35 Michigan St NE

      35 Michigan Street Northeast, Suite 3003, 
      Grand Rapids, MI 
      Experience:
      16+ years
      Languages Spoken:
      English

      Marian Bercu is a General Surgeon in Grand Rapids, Michigan. Dr. Bercu has been practicing medicine for over 16 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Lhermitte-Duclos Disease, Pediatric Low-Grade Glioma (pLGG), Processing Deficient Progeroid Laminopathies (PDPL), Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Deep Brain Stimulation.

      Learn about our expert tiers
      Jennifer L. Vanzee
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)

      Western Michigan Pediatrics PC - Grand Rapids

      721 Kenmoor Avenue Southeast, 
      Grand Rapids, MI 
      Experience:
      28+ years
      Languages Spoken:
      English
      Accepting New Patients

      Jennifer Vanzee is a Pediatrics provider in Grand Rapids, Michigan. Dr. Vanzee has been practicing medicine for over 28 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Obesity in Children, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Croup, and Autism Spectrum Disorder. Dr. Vanzee is currently accepting new patients.

      John N. Schuen
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Pediatric Pulmonology
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Pediatric Pulmonology

      Corewell Health Pediatric Sleep Disorders Clinic - Grand Rapids

      35 Michigan Street Northeast, Suite 3003, 
      Grand Rapids, MI 
      Experience:
      36+ years
      Languages Spoken:
      English
      Accepting New Patients

      John Schuen is a Pediatrics specialist and a Pediatric Pulmonologist in Grand Rapids, Michigan. Dr. Schuen has been practicing medicine for over 36 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Cystic Fibrosis, Laryngomalacia, Wolf-Hirschhorn Syndrome, and Periodic Limb Movement Disorder. Dr. Schuen is currently accepting new patients.

      Megan D. Quist
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)

      Corewell Health Pediatric Neurodevelopmental - Grand Rapids

      35 Michigan Street Northeast, Suite 3003, 
      Grand Rapids, MI 
      Experience:
      12+ years
      Languages Spoken:
      English

      Megan Quist is a Pediatrics provider in Grand Rapids, Michigan. Dr. Quist has been practicing medicine for over 12 years and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Autism Spectrum Disorder, Microcephaly, DiGeorge Syndrome, and Developmental Dysphasia Familial.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Cardiology
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Cardiology

      University Of Michigan Medical Center

      1500 E Medical Center Dr, 
      Ann Arbor, MI 
      Languages Spoken:
      English

      Courtney Strohacker is a Pediatric Cardiologist in Ann Arbor, Michigan. Dr. Strohacker is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Hypoplastic Left Heart Syndrome (HLHS), Mitral Atresia, Tetralogy of Fallot, Ventricular Septal Defects, and Patent Foramen Ovale Repair.

      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics

      Regents Of The University Of Michigan

      1500 E Medical Ctr Dr, 
      Ann Arbor, MI 
      Languages Spoken:
      English

      Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Maple Syrup Urine Disease.

      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics

      Regents Of The University Of Michigan

      1500 E Medical Ctr Dr, 
      Ann Arbor, MI 
      Languages Spoken:
      English
      Offers Telehealth

      Kristen Lee is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome.

      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Advanced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      35 Michigan St NE Ste 3003, 
      Grand Rapids, MI 
      Languages Spoken:
      English
      Accepting New Patients

      Stacie Adams is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency. Dr. Adams is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics

      Regents Of The University Of Michigan

      1500 E Medical Ctr, Suite 0331, 
      Ann Arbor, MI 
      Languages Spoken:
      English

      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 Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Nevoid Basal Cell Carcinoma Syndrome.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Medical Genetics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatrics | Medical Genetics

      Regents Of The University Of Michigan

      1500 E Medical Ctr, Suite 0331, 
      Ann Arbor, MI 
      Languages Spoken:
      English
      Offers Telehealth

      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 Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Aase Syndrome, Char Syndrome, Van Maldergem Syndrome, and C Syndrome.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Nephrology | Pediatrics | Nephrology
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Nephrology | Pediatrics | Nephrology

      Regents Of The University Of Michigan

      1500 E Medical Ctr, Suite 0331, 
      Ann Arbor, MI 
      Languages Spoken:
      English, German
      Accepting New Patients

      Matthias Wolf is a Pediatric Nephrologist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Wolf is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Fetal Thalidomide Syndrome, Pseudohypoaldosteronism Type 2, Liddle Syndrome, and Cystinosis. Dr. Wolf is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics

      Regents Of The University Of Michigan

      1105 6th St, 
      Traverse City, MI 
      Languages Spoken:
      English, Urdu
      Accepting New Patients

      Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Traverse City, Michigan. Dr. Ahmad is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Pulmonology | Pediatrics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Pediatric Pulmonology | Pediatrics
      1500 E Medical Center Dr, 
      Ann Arbor, MI 
      Languages Spoken:
      English
      Accepting New Patients

      Tara Havens is a Pediatric Pulmonologist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Havens is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Cystic Fibrosis, Congenital Unilateral Pulmonary Hypoplasia, Secondary Immunodeficiency (SID), and Newborn Jaundice. Dr. Havens is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics | Pediatrics

      Regents Of The University Of Michigan

      1500 E Medical Ctr, Suite 0331, 
      Ann Arbor, MI 
      Languages Spoken:
      English
      Accepting New Patients
      Offers Telehealth

      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 Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Delayed Growth, Cardiofaciocutaneous Syndrome, Noonan Syndrome, and Cardiomyopathic Lentiginosis. Dr. Ames is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Emergency Medicine | Pediatrics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Emergency Medicine | Pediatrics
      3621 S State St, 
      Ann Arbor, MI 
      Languages Spoken:
      English
      Accepting New Patients

      Matthew Lipshaw is an Emergency Medicine specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Lipshaw is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Croup, Genetic Epilepsy with Febrile Seizures Plus (GEFS+), Autism Spectrum Disorder, and Gastroschisis. Dr. Lipshaw is currently accepting new patients.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Medical Genetics

      Regents Of The University Of Michigan

      24 Frank Lloyd Wright Dr, Umhs Domino Farms, 
      Ann Arbor, MI 
      Languages Spoken:
      English

      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 Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia.

      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
      Experienced in Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)

      Mclaren Flint

      401 S Ballenger Hwy, Mclaren Flint 3 North, 
      Flint, MI 
      Languages Spoken:
      English
      Accepting New Patients
      Offers Telehealth

      Alexander Rodriguez is a primary care provider, practicing in Family Medicine in Flint, Michigan. Dr. Rodriguez is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Tracheitis, and Familial Chronic Mucocutaneous Candidiasis. Dr. Rodriguez is currently accepting new patients.

      Showing 1-19 of 19

      Last Updated: 01/09/2026

      What is the definition of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)?

      Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a condition that affects many different parts of the body. The condition occurs almost exclusively in boys, although it has been reported in a few girls. It is a progressively debilitating disorder; however, the rate of progression varies among affected individuals.

      When should I see a Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor in Michigan, US?

      There are various reasons why you may want to see a specialist, such as: 

      • Your primary care provider recommends it. 
      • Your condition requires expert knowledge and specialized care. 
      • Your symptoms persist or worsen despite treatment. 
      • You need specialized testing or procedures. 
      • You want a second opinion.  

      What should I consider when choosing a Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor in Michigan, US?

      It’s important to see a provider with expertise in your specific condition. Each provider profile in MediFind’s doctor database includes information on which conditions they treat, years of experience, research contributions, languages spoken, insurance plans accepted, and more.  

      How does MediFind rank Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctors in Michigan, US?

      MediFind’s rankings are based on a variety of data sources, such as the number of articles a doctor has published in medical journals, participation in clinical trials and industry conferences, as well as the number of patients that provider sees for a given condition. Note that MediFind’s provider database is not based on user reviews, and providers do not pay to be included in the database. 

      What types of insurance are accepted by Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctors in Michigan, US?

      Most profiles in MediFind’s doctor database include a list of insurance plans accepted by that provider. However, it’s a good idea to contact the provider’s office to make sure they still accept your insurance, then doublecheck by contacting your insurance plan to confirm they’re in network. 

      How can I book an appointment online with a Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor in Michigan, US?

      MediFind offers direct scheduling for certain providers using the “Request Appointment” button on that provider’s profile. If the schedule option is not available for a provider, tap the red “Show Phone Number” button on their profile to get their contact information. If you prefer to find providers who offer online scheduling, select “Schedules online” under the “Availability” category of the filter feature on the left side of the Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor search results page. 

      Why is it important to get a second opinion from a different Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor?

      Second opinions are an opportunity to confirm a diagnosis and its root cause, learn about alternative treatment options, or simply gain peace of mind. Many people, especially those with serious diagnoses, get second opinions so they can understand all their options and make informed decisions, so don’t hesitate to get one if you have any doubts or need more information or clarification regarding your care. Note that some insurance plans require second opinions, while others don’t cover second opinions, so be sure to confirm with your insurance provider first.   

      How can I prepare for my appointment with a Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor in Michigan, US?

      Prepare for your appointment by gathering the following items: 

      • Copies of medical records (dating back at least one year) 
      • Your medical history, including illnesses, medical conditions, surgeries, and other doctors you see 
      • Family history of disease 
      • List of current prescription drugs, over-the-counter medicines, vitamins, and herbal remedies or supplements including names and doses 
      • Allergies to medications, food, latex, insects, etc.  
      • List of questions and concerns 
      • Your insurance card 

      You might also contact the provider’s office to see if they offer transportation or childcare services or if you’re allowed to bring a loved one for support or to take notes during your visit. 

      What questions should I ask my Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor?

      Here are some sample questions: 

      • Can you explain in simple terms what this condition is and how it’s treated? 
      • What symptoms or side effects should I watch for? 
      • What tests will be involved, and when can I expect results? 
      • Are there other specialists I need to see? 
      • What’s the best way to reach you if I have follow-up questions? 

      How can I learn about the latest clinical trials and research advances my Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor may know about?

      MediFind’s Clinical Trials tool asks you a series of questions to help you narrow down your search by health condition, age, gender, location, how far you’re willing to travel, and more. Each question you answer filters down the number of trials until you find the ones that are most relevant to you. 

      MediFind’s Latest Advances tool features summaries of recent articles published in medical journals. We use cutting-edge technology to scour medical publication databases for the latest research advancements on any given condition, then we simplify this information in a way that’s useful and easy to understand. 

      Can I filter my search to show male or female Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctors in Michigan, US?

      Look for the filter feature on the left side of the Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor search results page. Select “Female” or “Male” under the “Gender” category to search for female or male providers exclusively. If the “Any” option is selected, it will pull results for both male and female providers. 

      Can I filter my search to find a Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor that offers video calls?

      Look for the filter feature on the left-side of the Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome) doctor search results page. Select “Offers telehealth visits” under the Availability category to search for providers who offer virtual appointments (video calls). 

      Reviewed on: 11/11/24  

      By: MediFind Medical Staff 

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