The 20 Best PEPCK 1 Deficiency Doctors Near Me in Michigan, US

Find the Top PEPCK 1 Deficiency Experts and Specialists

Last Updated: 09/19/2026

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MediFind found 23 doctor with experience in PEPCK 1 Deficiency near Michigan, US. Of these, 19 are Experienced and 4 are Advanced.

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23 providers found
    Advanced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Advanced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Referral may be required

    U Of M Neurology

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

    Steven Leber is a Pediatric Neurologist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Leber is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Myoclonic Epilepsy, Seizures, Partial Seizure, and Dihydrolipoamide Dehydrogenase Deficiency. Dr. Leber is currently accepting new patients.

    Advanced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Advanced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Referral may be required

    University Of Michigan Pediatric Genetics Clinic

    1540 East Hospital Drive, Floor 6, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    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 PEPCK 1 Deficiency. 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.

    Advanced in PEPCK 1 Deficiency
    Pediatrics | Medical Genetics
    Advanced in PEPCK 1 Deficiency
    Pediatrics | Medical Genetics
    Referral may be required

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

    25 Michigan Street Northeast, Suite 2100, 
    Grand Rapids, MI 
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. 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.

    Learn about our expert tiers
    Experienced in PEPCK 1 Deficiency
    Experienced in PEPCK 1 Deficiency
    Referral may be required

    Serenity Pediatrics

    71 E. Long Lake Rd, 
    Bloomfield Hills, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Emily Casterline is a Pediatrics provider practicing medicine in Bloomfield Hills, Michigan. Dr. Casterline is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Obesity in Children, Croup, Herpangina, and Delayed Growth. Dr. Casterline is board certified in American Osteopathic Board Of Pediatrics. Dr. Casterline is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Experienced in PEPCK 1 Deficiency
    Referral may be required

    Serenity Pediatrics

    71 E. Long Lake Rd, 
    Bloomfield Hills, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Jennifer Cohen is a Pediatrics provider practicing medicine in Bloomfield Hills, Michigan. Dr. Cohen is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Obesity in Children, Delayed Growth, Autism Spectrum Disorder, and PEPCK 1 Deficiency. Dr. Cohen is board certified in American Board Of Pediatrics. Dr. Cohen is currently accepting new patients.

    Advanced in PEPCK 1 Deficiency
    Advanced in PEPCK 1 Deficiency
    Referral may be required

    Office

    1540 E Medical Center Dr # 12-733, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Sucheta Joshi is a Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Joshi is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 29 other conditions, according to our data. Her clinical expertise encompasses West Syndrome, Epilepsy in Children, Epilepsy, and Seizures. Dr. Joshi is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Referral may be required

    Corewell Health Pediatric Neurology - 35 Michigan St NE

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

    Caitlin Groeneveld is a Nurse Practitioner practicing medicine in Grand Rapids, Michigan. Groeneveld, NP is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her clinical expertise encompasses PEPCK 1 Deficiency, Dihydrolipoamide Dehydrogenase Deficiency, Autosomal Recessive Congenital Methemoglobinemia, and Pyruvate Carboxylase Deficiency. Groeneveld, NP is board certified in Pediatric Nursing Certification Board. Groeneveld, NP is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Referral may be required

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English

    Jessica Rieckhoff is a Nurse Practitioner practicing medicine in Ann Arbor, Michigan. Rieckhoff, NP is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her clinical expertise encompasses Autosomal Recessive Congenital Methemoglobinemia, Pyruvate Carboxylase Deficiency, PEPCK 1 Deficiency, and Dihydrolipoamide Dehydrogenase Deficiency. Rieckhoff, NP is board certified in Acute Care Pediatric Nurse Pract.

    Experienced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Experienced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Referral may be required

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English, Urdu
    Accepting New Patients

    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 PEPCK 1 Deficiency. 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.

    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Referral may be required

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Julie Ziobro is a Pediatric Neurologist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ziobro is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Seizures, Generalized Tonic-Clonic Seizure, Myoclonic Epilepsy, and Absence Seizure. Dr. Ziobro is board certified in Epilepsy and Neurology W/Spec Qual Child Neuro. Dr. Ziobro is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Experienced in PEPCK 1 Deficiency
    Referral may be required

    Corewell Health Pediatric Ophthalmology - 35 Michigan St NE

    35 Michigan Street Northeast, Suite 5101, 
    Grand Rapids, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Lauren Fletcher-Morehouse is a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Fletcher-Morehouse is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Neurofibromatosis, Gomez Lopez Hernandez Syndrome, Marcus Gunn Phenomenon, and Legius Syndrome. Dr. Fletcher-Morehouse is board certified in American Osteopathic Board Of Ophthalmology & Otolaryngology. Dr. Fletcher-Morehouse is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology | Pediatrics
    Referral may be required

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Martha Carlson is a Pediatric Neurologist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Carlson is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Autism Spectrum Disorder, Spasmus Nutans, Seizures, and Adrenoleukodystrophy (ALD). Dr. Carlson is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Pediatrics | Neurology | Pediatric Neurology
    Experienced in PEPCK 1 Deficiency
    Pediatrics | Neurology | Pediatric Neurology
    Referral required

    Pediatric Neurology Clinic

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Eric Armour is a Pediatrics specialist and a Neurologist practicing medicine in Ann Arbor, Michigan. Dr. Armour is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. He is also highly rated in 34 other conditions, according to our data. His clinical expertise encompasses Seizures, Generalized Tonic-Clonic Seizure, Tuberous Sclerosis Complex, and Tuberous Sclerosis. Dr. Armour is board certified in Epilepsy, Clinical Neurophysiology, and Neurology W/Spec Qual Child Neuro. Dr. Armour is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Experienced in PEPCK 1 Deficiency
    Referral may be required

    Oakwood Family Center

    18501 Rotunda Drive, Suite 200, 
    Dearborn, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Susan Youngs is a Pediatrics provider practicing medicine in Dearborn, Michigan. Dr. Youngs is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Rasmussen Encephalitis, Autism Spectrum Disorder, Early Infantile Epileptic Encephalopathy, and Microcephaly Deafness Syndrome. Dr. Youngs is board certified in American Board Of Physical Medicine And Rehabilitation and American Board Of Pediatrics. Dr. Youngs is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology
    Experienced in PEPCK 1 Deficiency
    Pediatric Neurology
    Referral may be required

    Corewell Health Pediatric Neurology - Munson Ave, Traverse City

    880 Munson Avenue, Suite H, 
    Traverse City, MI 
    Languages Spoken:
    English, Russian
    Accepting New Patients

    Anastasia Luniova is a Pediatric Neurologist practicing medicine in Traverse City, Michigan. Dr. Luniova is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 17 other conditions, according to our data. Her clinical expertise encompasses Seizures, Epilepsy in Children, Absence Seizure, and Myoclonic Epilepsy. Dr. Luniova is board certified in American Board Of Psychiatry And Neurology, Neurology With Special Qualification In Child Neurology - 2014, American Board Of Psychiatry And Neurology, American Board Of Psychiatry And Neurology, Epilepsy - 2017 , and American Board Of Psychiatry And Neurology, Clinical Neurophysiology - 2015 . Dr. Luniova is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Pediatrics | Pediatric Neurology
    Experienced in PEPCK 1 Deficiency
    Pediatrics | Pediatric Neurology
    Referral may be required

    Corewell Health William Beaumont University Hospital Adult Neurosurgery Florence & Richard McBrien Pediatric Neuroscience Center - 3555 W 13 Mile Rd

    3555 West 13 Mile Road, Suite N300, 
    Royal Oak, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Nancy Mcnamara is a Pediatrics specialist and a Pediatric Neurologist practicing medicine in Royal Oak, Michigan. Dr. Mcnamara is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. She is also highly rated in 16 other conditions, according to our data. Her clinical expertise encompasses Seizures, Epilepsy in Children, Generalized Tonic-Clonic Seizure, and Lennox-Gastaut Syndrome (LGS). Dr. Mcnamara is board certified in American Board Of Psychiatry And Neurology. Dr. Mcnamara is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Pediatric Surgery | General Surgery
    Experienced in PEPCK 1 Deficiency
    Pediatric Surgery | General Surgery
    Referral may be required

    Brighton Center For Specialty Care

    7500 Challis Rd, Entrance 1 Level 2, 
    Brighton, MI 
    Languages Spoken:
    English, Telugu
    Accepting New Patients

    Samir Gadepalli is a Pediatric Surgeon and a General Surgeon practicing medicine in Brighton, Michigan. Dr. Gadepalli is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Omphalocele, Tracheoesophageal Fistula, Donnai-Barrow Syndrome, Appendectomy, and Ileostomy. Dr. Gadepalli is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Experienced in PEPCK 1 Deficiency
    Nurse Practitioner
    Referral may be required

    Corewell Health Pediatric Pain And Palliative Care 5301 - 35 Michigan St NE

    35 Michigan Street Northeast, Suite 5301, 
    Grand Rapids, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Sandra Vanbrouwer is a Nurse Practitioner practicing medicine in Grand Rapids, Michigan. Vanbrouwer, NP is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her clinical expertise encompasses Wolf-Hirschhorn Syndrome, Koolen De Vries Syndrome, Dihydrolipoamide Dehydrogenase Deficiency, and PEPCK 1 Deficiency. Vanbrouwer, NP is board certified in Pediatric Nursing Certification Board and American Nurses Credentialing Center (ANCC). Vanbrouwer, NP is currently accepting new patients.

    Experienced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Experienced in PEPCK 1 Deficiency
    Medical Genetics | Pediatrics
    Referral may be required

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 6 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    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 PEPCK 1 Deficiency. 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.

    Experienced in PEPCK 1 Deficiency
    Family Medicine
    Experienced in PEPCK 1 Deficiency
    Family Medicine

    Ascension Genesys Hospital

    1 Genesys Pkwy, 
    Grand Blanc, MI 
    Languages Spoken:
    English
    Accepting New Patients

    Michael Schwartz is a primary care provider, practicing in Family Medicine in Grand Blanc, Michigan. Dr. Schwartz is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Obesity, Type 2 Diabetes (T2D), Low Blood Sugar, and Maturity Onset Diabetes of the Young. Dr. Schwartz is currently accepting new patients.

    Showing 1-20 of 23

    Last Updated: 09/19/2026

    What is the definition of PEPCK 1 Deficiency?

    PEPCK1 deficiency is a rare inborn error of metabolism disorder, characterized by the deficiency of the enzyme PEPCK1, one of the enzymes needed for gluconeogenesis, the process by which organisms produce sugars (namely glucose) from non-carbohydrate precursors (such as amino acids). In severe cases, symptoms may include persistent and very low levels of blood's sugar in newborns (neonatal hypoglycemia), failure to thrive, build-up of lactic acid in the blood (lactic acidosis), liver enlargement (hepatomegaly) and liver failure leading to neurological degeneration. Milder cases present during childhood with fewer and less serious liver problems. Infections and fasting may trigger the symptoms. PEPCK1 deficiency inheritance is autosomal recessive. It is caused by genetic changes in the PEPCK1 gene. PEPCK1 is the cytosolic form of the phosphoenolpyruvate carboxykinase (PEPCK) enzyme, the other being the mitochondrial (PEPCK2).

    When should I see a PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency doctor search results page. 

    Why is it important to get a second opinion from a different PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency 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 PEPCK 1 Deficiency doctors in Michigan, US?

    Look for the filter feature on the left side of the PEPCK 1 Deficiency 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 PEPCK 1 Deficiency doctor that offers video calls?

    Look for the filter feature on the left-side of the PEPCK 1 Deficiency 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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