The 20 Best Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency Doctors in The United States

Find the Top Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 99 doctor with experience in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency near The United States. Of these, 58 are Experienced, 39 are Advanced and 2 are Distinguished.

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99 providers found
    Distinguished in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Distinguished in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency

    Washington University

    660 S Euclid Ave, 
    Saint Louis, MO 
    Languages Spoken:
    English

    Peter Crawford is a Cardiologist practicing medicine in Saint Louis, Missouri. Dr. Crawford is rated as a Distinguished provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Heart Failure, and Hereditary Ataxia.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics

    St. Christopher's Pediatric Associates Genetics - E. Erie Avenue

    160 E Erie Ave, 
    Philadelphia, PA 
    Languages Spoken:
    English

    . Dr. Perszyk is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency

    Medical Genetics Metabolic In Lawrenceville

    4401 Penn Avenue, 
    Pittsburgh, PA 
    Languages Spoken:
    English
    Offers Telehealth

    Gerard (Jerry) Vockley MD, PhD, is a medical geneticist and is certified in clinical genetics and biochemical and molecular genetics by the American Board of Medical Genetics and Genomics. He is chief of the Division of Medical Genetics, director of the Center for Rare Disease Therapy, and is the Cleveland Family Endowed Professor of pediatric research at the University of Pittsburgh School of Medicine. He completed his medical degree and PhD at the University of Pennsylvania and completed his residency at the University of Colorado, followed by his fellowship at Yale University School of Medicine. Dr. Vockley is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, and Arginase Deficiency. Dr. Vockley is board certified in American Board Of Medical Genetics And Genomics and American Board Of Medical Genetics And Genomics.

    Learn about our expert tiers
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Cardiology | Pediatrics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Cardiology | Pediatrics

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 11 Reception C, 
    Ann Arbor, MI 
    Languages Spoken:
    English

    David Bradley is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Bradley is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Transposition of the Great Arteries, Tetralogy of Fallot, Congenital Heart Block, and Hypoplastic Left Heart Syndrome (HLHS).

    Distinguished in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Internal Medicine
    Distinguished in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Internal Medicine

    Office

    1000 Waterman Way, 
    Tavares, FL 
    Languages Spoken:
    English

    Joseph Risko is a primary care provider, practicing in Internal Medicine in Tavares, Florida. Dr. Risko is rated as a Distinguished provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Necrosis, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Hypertensive Heart Disease, Colonoscopy, and Pacemaker Implantation.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Endocrinology
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Endocrinology

    Mt Endocrinology PC

    984 N Broadway Ste 305, 
    Yonkers, NY 
    Languages Spoken:
    English
    Offers Telehealth

    Maggie Tavdy is an Endocrinologist practicing medicine in Yonkers, New York. Dr. Tavdy is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Thyroid Nodule, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), and Hypothyroidism.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics

    UT Southwestern - Pediatrics

    5323 Harry Hines Blvd, 
    Dallas, TX 
    Languages Spoken:
    English, Spanish

    Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics
    1201 West La Veta Avenue, 
    Orange, CA 
    Languages Spoken:
    English
    Accepting New Patients

    Cristel Chapel is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chapel is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses CLN4 Disease, CLN2 Disease, CLN3 Disease, and CLN5 Disease. Dr. Chapel is currently accepting new patients.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency

    Vanderbilt University

    2200 Childrens Way, 
    Nashville, TN 
    Languages Spoken:
    English
    Offers Telehealth

    Jenna Essakow is a Pediatrics provider practicing medicine in Nashville, Tennessee. Dr. Essakow is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Emergency Medicine
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Emergency Medicine

    Sentara Pulmonary, Critical Care & Sleep Specialists

    600 Gresham Dr Ste 8630B, 
    Norfolk, VA 
    Languages Spoken:
    English

    Michael Hooper is an Emergency Medicine provider practicing medicine in Norfolk, Virginia. Dr. Hooper is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Pulmonary Veno-Occlusive Disease, Pulmonary Hypertension, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Cystic Fibrosis, and Endoscopy.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency

    Connecticut Children's

    282 Washington St, 
    Hartford, CT 
    Languages Spoken:
    English

    Richard Pierce is a Pediatrics provider practicing medicine in Hartford, Connecticut. Dr. Pierce is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency and Multisystem Inflammatory Syndrome in Children (MIS-C).

    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Endocrinology | Pediatrics
    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Endocrinology | Pediatrics

    C. S. Mott Children's Hospital

    1540 E Hospital Dr, Floor 8 Reception B, 
    Ann Arbor, MI 
    Languages Spoken:
    English

    David Olson earned his M.D. and Ph.D. at the University of Michigan (the latter in Cellular and Molecular Biology). He served his internship and residency at Children’s Hospital Boston, followed by a fellowship in pediatric endocrinology and metabolism at Children’s Hospital Boston/Joslin Diabetes Center. Prior to returning to the University of Michigan, Dr. Olson was on staff at Children's Hospital Boston and affiliated with the Department of Newborn Medicine at Brigham and Women’s Hospital. His postdoctoral research was performed at Beth Israel Deaconess Medical Center, Division of Endocrinology. Using novel mouse models, Dr. Olson is exploring gene expression changes in specific neuronal populations in the brain that are known to be important in regulating energy balance; these studies are directed at examining the link between gene expression in specific areas of the brain and altered metabolism. Additional studies using neuron-specific genetic changes are underway to clarify the molecular basis of daily biologic rhythms and explore how disruption of these rhythms predisposes organisms (rodents and humans) to pathologic changes in metabolism. Dr. Olson is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Type 1 Diabetes (T1D), Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), and Familial Short Stature (FSS). Dr. Olson is board certified in Pediatric Endocrinology.

    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Ophthalmology
    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Ophthalmology
    259 E Erie St Ste 1520, Lavin Family Pavilion, 
    Chicago, IL 
    Experience:
    8+ years
    Languages Spoken:
    English

    David Ramirez is an Ophthalmologist practicing medicine in Chicago, Illinois. He has been practicing medicine for over 8 years. Dr. Ramirez is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Strabismus, Amblyopia, Papilledema, and Esotropia. Dr. Ramirez is board certified in American Board Of Ophthalmology - Ophthalmology (Certified).

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Internal Medicine
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Internal Medicine

    517 Moye Medical Center-Adult And Pediatric Health Care

    517 Moye Blvd Fl Second, 
    Greenville, NC 
    Languages Spoken:
    English
    Offers Telehealth

    Lacy Hobgood is a primary care provider, practicing in Internal Medicine in Greenville, North Carolina. Dr. Hobgood is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Type 2 Diabetes (T2D), Familial Hypertension, Endoscopy, and Gastrostomy.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics

    C. S. Mott Children's Hospital

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

    Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. 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.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Family Medicine | Internal Medicine
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Family Medicine | Internal Medicine

    Domino's Farms

    24 Frank Lloyd Wright Dr Ste 1300, Lobby C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Offers Telehealth

    Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. 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.

    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics
    Advanced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Medical Genetics | Pediatrics

    Domino's Farms

    24 Frank Lloyd Wright Dr Ste 1300, Lobby C, 
    Ann Arbor, MI 
    Languages Spoken:
    English
    Offers Telehealth

    Dr. Lee earned her M.D. from Ross University School of Medicine in 2013, and completed Pediatric Residency at Ascension St. John Hospital in Grosse Point, MI, where she served as a Chief Pediatric Resident during her final year of residency. She completed Categorical Medical Genetics Residency at the University of Michigan in 2019. Following this she accepted a dual faculty position as a Clinical Lecturer in the Department of Pediatrics and Department of Internal Medicine for one year, before returning to Fellowship in 2020 to complete additional dedicated training in Medical Biochemical Genetics. After completion of Medical Biochemical Genetics Fellowship, she resumed her faculty position as a Clinical Assistant Professor in 2021. She is board certified in Pediatrics, and in Clinical and General Genetics.She has a dual faculty appointment in the Department of Pediatrics and the Department of Internal Medicine. As a faculty member in the Department of Pediatrics, she sees patients in the Pediatric Genetics and Biochemical Genetics Clinics, in addition to the newly created Multidisciplinary Genetics of Hearing Loss Clinic. As a faculty member in the Department of Internal Medicine, she sees patients in the Adult Medical Genetics and Cancer Genetics Clinics, in addition to patients with atypical diabetes and/or lipodystrophy in collaboration with MEND.In addition to her clinical responsibilities, Dr. Lee also enjoys spending time teaching and discussing various aspects of genetics with fellows, pediatric residents, medical students, and genetic counseling students. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. 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, Clinical Genetics & Genomics, and Medical Biochemical Genetics.

    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Cardiology
    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatric Cardiology

    Children's Mercy Kansas City

    2401 Gillham Rd, 
    Kansas City,, MO 
    Languages Spoken:
    English

    Nitin Madan is a Pediatric Cardiologist practicing medicine in Kansas City,, Missouri. Dr. Madan is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Congenital Coronary Artery Malformation, Anomalous Left Coronary Artery from the Pulmonary Artery, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.

    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatrics | Medical Genetics
    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Pediatrics | Medical Genetics

    UT Southwestern - Pediatric Genetics

    1935 Medical District Dr, 
    Dallas, TX 
    Languages Spoken:
    English

    Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Scheuerle is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 170 other conditions, according to our data. Her clinical expertise encompasses Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.

    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Neurology
    Experienced in Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
    Neurology

    Ann & Robert H. Lurie Children's Hospital Of Chicago

    225 E Chicago Ave, 
    Chicago, IL 
    Languages Spoken:
    English

    Joyce Wu is a Neurologist practicing medicine in Chicago, Illinois. Dr. Wu is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Epilepsy in Children, Autism Spectrum Disorder, Orofaciodigital Syndrome 6, and Hydranencephaly.

    Showing 1-20 of 99

    Last Updated: 04/28/2026

    What is the definition of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency?

    Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is an inherited disorder that impairs the body's ability to break down ketones, which are molecules produced in the liver during the breakdown of fats.

    When should I see a Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctors in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctors in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor search results page. 

    Why is it important to get a second opinion from a different Succinyl-CoA:3-Ketoacid CoA Transferase 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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor in The United States?

    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 Succinyl-CoA:3-Ketoacid CoA Transferase 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 Succinyl-CoA:3-Ketoacid CoA Transferase 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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctors in The United States?

    Look for the filter feature on the left side of the Succinyl-CoA:3-Ketoacid CoA Transferase 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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency doctor that offers video calls?

    Look for the filter feature on the left-side of the Succinyl-CoA:3-Ketoacid CoA Transferase 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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