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    Last Updated: 03/06/2025

     
     
     
     
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    MediFind found 32 doctor with experience in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Of these, 19 are Advanced, 11 are Experienced and 1 are Distinguished.

    Location:
    32 providers found
    Distinguished in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Distinguished in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    One Gustave Levy L. Place #1497, 
    New York, NY 
     (512.6 mi)
    Languages Spoken:
    English

    George Diaz is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Diaz and is rated as a Distinguished provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Inborn Amino Acid Metabolism Disorder, and Ornithine Translocase Deficiency.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    Children's Hospital Medical Center

    3333 Burnet Ave, 
    Cincinnati, OH 
     (157.3 mi)
    Languages Spoken:
    English
    Accepting New Patients

    Nancy Leslie is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Leslie and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Pompe Disease, Ornithine Transcarbamylase Deficiency, Argininosuccinic Aciduria, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Dr. Leslie is currently accepting new patients.

    What does Elite, Distinguished, Advanced, Experienced mean?
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    University Of Virginia Physicians Group

    1204 W Main St, 
    Charlottesville, VA 
     (223.0 mi)
    Languages Spoken:
    English
    Offers Telehealth

    William Wilson is a Medical Genetics specialist and a Pediatrics provider in Charlottesville, Virginia. Dr. Wilson and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Danon Disease, Pompe Disease, Propionic Acidemia, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

    Learn about our expert tiers
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    University Family Physicians, Inc.

    975 W Walnut St, 
    Indianapolis, IN 
     (253.3 mi)
    Languages Spoken:
    English
    Accepting New Patients

    Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Hainline and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Phenylketonuria (PKU), Adrenoleukodystrophy (ALD), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Hainline is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    The Emory Clinic Inc

    1365 Clifton Rd Ne, 
    Atlanta, GA 
     (274.1 mi)
    Languages Spoken:
    English, Arabic, Italian, Portuguese, Spanish
    Accepting New Patients

    William Wilcox is a Medical Genetics specialist and a Pediatrics provider in Atlanta, Georgia. Dr. Wilcox and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Multiple Sulfatase Deficiency. Dr. Wilcox is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Neonatology | Medical Genetics | Obstetrics and Gynecology
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Neonatology | Medical Genetics | Obstetrics and Gynecology

    Pediatrix Medical Group Of The Mid-Atlantic PC

    400 W 7th St, 
    Frederick, MD 
     (307.1 mi)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Donna Raval is a Neonatologist and a Medical Genetics provider in Frederick, Maryland. Dr. Raval and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency and Premature Infant. Dr. Raval is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Nhgri 10 Center Dr Bldg 10, Rm 10c103, 
    Bethesda, MD 
     (311.8 mi)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Meral Gunay-Aygun is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gunay-Aygun and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Argininosuccinic Aciduria. Dr. Gunay-Aygun is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    1500 E Medical Center Dr, 
    Ann Arbor, MI 
     (338.0 mi)
    Languages Spoken:
    English
    Accepting New Patients

    Jess Thoene is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Thoene and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Inborn Amino Acid Metabolism Disorder, and Glycine Encephalopathy. Dr. Thoene is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    Johns Hopkins University

    601 N Caroline St, 
    Baltimore, MD 
     (344.4 mi)
    Experience:
    40+ years
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Ada Hamosh is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Hamosh has been practicing medicine for over 40 years and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, and Propionic Acidemia. Dr. Hamosh is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics

    Johns Hopkins University

    600 N Wolf St, 
    Baltimore, MD 
     (344.6 mi)
    Experience:
    21+ years
    Languages Spoken:
    English

    Hilary Vernon is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Vernon has been practicing medicine for over 21 years and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Inborn Amino Acid Metabolism Disorder, and Progressive External Ophthalmoplegia.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    Washington University

    1 Childrens Pl, 
    Saint Louis, MO 
     (428.8 mi)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Marwan Shinawi is a Medical Genetics specialist and a Pediatrics provider in Saint Louis, Missouri. Dr. Shinawi and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Hypotonia, Polysyndactyly Cardiac Malformation, Osteopathia Striata Cranial Sclerosis, and Increased Head Circumference. Dr. Shinawi is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    University Of Wisconsin Medical Foundation Inc

    1500 Highland Ave, 
    Madison, WI 
     (531.2 mi)
    Languages Spoken:
    English
    Accepting New Patients

    William Rhead is a Medical Genetics specialist and a Pediatrics provider in Madison, Wisconsin. Dr. Rhead and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Gaucher Disease Type 1, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Rhead is currently accepting new patients.

    Nadia A. Falah
    Medical Genetics
    Medical Genetics

    MD Genetic Clinic

    1201 6th Ave W, 
    Bradenton, FL 
     (689.9 mi)
    Experience:
    9+ years
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Dr. Falah is a Medical Doctor specializing in Medical Genetics and Metabolic Disorders. She is a former assistant professor in the Department of Pediatrics, Division of Genetics and Metabolism, at West Virginia University. Additionally, she previously served on the West Virginia Advisory Council on Rare Diseases, with a particular focus on rare diseases.Dr. Falah earned her medical degree from Tripoli University of Medical Science in Tripoli, Libya. She then completed a residency in clinical genetics at the University of Miami Leonard M. Miller School of Medicine/Jackson Health System. Following this, Dr. Falah pursued a fellowship in clinical pharmacology at the Indiana University School of Medicine/IU Health. She also holds a Master of Science degree in Clinical Investigation from Vanderbilt University in Nashville, Tennessee. To further advance her expertise in genetics, she completed a medical biochemical fellowship at Duke University.Dr. Falah is board-certified in Medical Genetics and Medical Biochemical Genetics by the American Board of Medical Genetics and Genomics (ABMGG). She has been a member of the American College of Medical Genetics and Genomics and the American Medical Association since 2014. Dr. Falah’s work has been published in peer-reviewed journals, and she has presented at various medical conferences. She also serves as a reviewer for several medical journals and as a consultant for private pharmaceutical companies. . Her top areas of expertise are Prostate Cancer, Familial Prostate Cancer, 46XX Testicular Disorder of Sex Development, and Pelizaeus-Merzbacher Disease.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    Fairview Express Care

    717 Delaware St Se, Suite 340, 
    Minneapolis, MN 
     (758.9 mi)
    Experience:
    47+ years
    Languages Spoken:
    English
    Accepting New Patients

    Susan Berry is a Medical Genetics specialist and a Pediatrics provider in Minneapolis, Minnesota. Dr. Berry has been practicing medicine for over 47 years and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Propionic Acidemia, Argininosuccinic Aciduria, Autosomal Recessive Congenital Methemoglobinemia, and Ornithine Translocase Deficiency. Dr. Berry is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics | Pediatric Endocrinology
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics | Pediatric Endocrinology

    Sanford Medical Center

    1205 S Grande Ave, Suite 510, 
    Sioux Falls, SD 
     (854.7 mi)
    Languages Spoken:
    English
    Accepting New Patients

    Laura Davis-Keppen is a Medical Genetics specialist and a Pediatrics provider in Sioux Falls, South Dakota. Dr. Davis-Keppen and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Danon Disease, and Pompe Disease. Dr. Davis-Keppen is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    28013 E Nova Pl, 
    Aurora, CO 
     (1205.0 mi)
    Experience:
    14+ years
    Languages Spoken:
    English
    Accepting New Patients

    Jessica Duis is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Duis has been practicing medicine for over 14 years and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Angelman Syndrome, Prader-Willi Syndrome, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Hypotonia, and Gastrostomy. Dr. Duis is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Geriatrics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Geriatrics | Pediatrics

    Uc Regents

    10833 Leconte Ave, 
    Los Angeles, CA 
     (2015.4 mi)
    Languages Spoken:
    English

    Derek Wong is a Medical Genetics specialist and a Geriatrics provider in Los Angeles, California. Dr. Wong and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Von Gierke Disease, Argininosuccinic Aciduria, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Medical Genetics | Pediatrics

    Uc Regents

    10833 Le Conte Ave, 
    Los Angeles, CA 
     (2015.4 mi)
    Languages Spoken:
    English, Hindi, Italian, Spanish
    Accepting New Patients
    Offers Telehealth

    Nicola Longo is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Longo and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Primary Carnitine Deficiency, Gaucher Disease Type 1, Urea Cycle Disorders (UCD), and Phenylketonuria (PKU). Dr. Longo is currently accepting new patients.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics

    Valley Childrens Medical Group

    9300 Valley Childrens Pl, 
    Madera, CA 
     (2039.1 mi)
    Languages Spoken:
    English

    Susan Winter is a Pediatrics specialist and a Medical Genetics provider in Madera, California. Dr. Winter and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Phenylketonuria (PKU), and Methylmalonic Acidemia.

    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics
    Advanced in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
    Pediatrics | Medical Genetics
    4800 Sand Point Way Ne, M/s Mb.8.632, 
    Seattle, WA 
     (2115.3 mi)
    Languages Spoken:
    English, Hindi
    Accepting New Patients
    Offers Telehealth

    Christina Lam is a Pediatrics specialist and a Medical Genetics provider in Seattle, Washington. Dr. Lam and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Inborn Amino Acid Metabolism Disorder, and Urea Cycle Disorders (UCD). Dr. Lam is currently accepting new patients.

    Showing 1-20 of 32

    Last Updated: 03/06/2025

    What is the definition of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency?

    3-hydroxy-3-methylglutaryl-CoA lyase deficiency (also known as HMG-CoA lyase deficiency) is an uncommon inherited disorder in which the body cannot process a particular protein building block (amino acid) called leucine. Additionally, the disorder prevents the body from making ketones, which are compounds that are used for energy during periods without food (fasting).

    When should I see a 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctors near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctors near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor search results page. 

    Why is it important to get a second opinion from a different 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor near me?

    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 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctors near me?

    Look for the filter feature on the left side of the 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency doctor that offers video calls?

    Look for the filter feature on the left-side of the 3-Hydroxy-3-Methylglutaryl-CoA Lyase 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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