The 20 Best PMM2-Congenital Disorder of Glycosylation Doctors in Mexico

Find the Top PMM2-Congenital Disorder of Glycosylation Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 13 doctor with experience in PMM2-Congenital Disorder of Glycosylation near Mexico. Of these, 12 are Experienced and 1 are Advanced.

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13 providers found
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Ivan Duncker-Martinez
    Advanced in PMM2-Congenital Disorder of Glycosylation

    Ivan Duncker-Martinez
    Cuernavaca, MOR, MX 

    Ivan Duncker-Martinez practices practicing medicine in Cuernavaca, Mexico. Mr. Duncker-Martinez is rated as an Advanced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Sporotrichosis, ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, and Adult Polyglucosan Body Disease.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Roberta Marin-Salinas
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Roberta Marin-Salinas
    Cuernavaca, MOR, MX 

    Roberta Marin-Salinas practices practicing medicine in Cuernavaca, Mexico. Ms. Marin-Salinas is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Sporotrichosis, and Limb-Girdle Muscular Dystrophy.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Luis L. Lagunes-Flores
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Luis L. Lagunes-Flores
    Mexico City, DIF, MX 

    Luis Lagunes-Flores practices practicing medicine in Mexico City, Mexico. Mr. Lagunes-Flores is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Acute Lymphoblastic Leukemia (ALL), and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome).

    Learn about our expert tiers
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carmen Verson-Alaez
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carmen Verson-Alaez
    Mexico City, DIF, MX 

    Carmen Verson-Alaez practices practicing medicine in Mexico City, Mexico. Ms. Verson-Alaez is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Dihydrolipoamide Dehydrogenase Deficiency, and Cytochrome C Oxidase Deficiency.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Karol Sanchez-Carrillo
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Karol Sanchez-Carrillo
    Mexico City, DIF, MX 

    Karol Sanchez-Carrillo practices practicing medicine in Mexico City, Mexico. Sanchez-Carrillo is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Dihydrolipoamide Dehydrogenase Deficiency, and Maple Syrup Urine Disease.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Marco Olivares-Jimenez
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Marco Olivares-Jimenez
    Mexico City, DIF, MX 

    Marco Olivares-Jimenez practices practicing medicine in Mexico City, Mexico. Mr. Olivares-Jimenez is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Cytochrome C Oxidase Deficiency, and Amenorrhea.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carolina Garay-Molina
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Carolina Garay-Molina
    Mexico City, DIF, MX 

    Carolina Garay-Molina practices practicing medicine in Mexico City, Mexico. Ms. Garay-Molina is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Cytochrome C Oxidase Deficiency, and Childhood Acute Myeloid Leukemia.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Camilo E. Villarroel
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Camilo E. Villarroel
    Mexico, MEX, MX 

    Camilo Villarroel practices practicing medicine in Mexico, Mexico. Mr. Villarroel is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Lenz Microphthalmia Syndrome, Microphthalmia, De Barsy Syndrome, and Peters Anomaly.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mario E. Munoz-Cruz
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Mario E. Munoz-Cruz
    Cuernavaca, MOR, MX 

    Mario Munoz-Cruz practices practicing medicine in Cuernavaca, Mexico. Mr. Munoz-Cruz is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses ALG1-CDG, Omenn Syndrome, Piebaldism, and Mononucleosis.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Miguel Morales-Rodriguez
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Miguel Morales-Rodriguez
    Mexico City, DIF, MX 

    Miguel Morales-Rodriguez practices practicing medicine in Mexico City, Mexico. Mr. Morales-Rodriguez is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses Vici Syndrome, Corpus Callosum Agenesis, Disseminated Tuberculosis, and Cervical Cancer.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Felipe Rodriguez-Olvera
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Felipe Rodriguez-Olvera
    C.P. 62210 Cuernavaca, Mor, 
    Cuernavaca, MOR, MX 

    Felipe Rodriguez-Olvera practices practicing medicine in Cuernavaca, Mexico. Mr. Rodriguez-Olvera is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. His clinical expertise encompasses PMM2-Congenital Disorder of Glycosylation and Breast Cancer.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hector M. Montes-Mora
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Hector M. Montes-Mora
    Noria Alta S/n, C.P, 
    Noria Alta, GUA, MX 

    Hector Montes-Mora practices practicing medicine in Noria Alta, Mexico. Mr. Montes-Mora is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Sporotrichosis, ALG1-CDG, Shingles, and PMM2-Congenital Disorder of Glycosylation.

    Experienced in PMM2-Congenital Disorder of Glycosylation

    Anallely Rivas-Munoz
    Experienced in PMM2-Congenital Disorder of Glycosylation

    Anallely Rivas-Munoz
    Mexico City, DIF, MX 

    Anallely Rivas-Munoz practices practicing medicine in Mexico City, Mexico. Ms. Rivas-Munoz is rated as an Experienced expert by MediFind in the treatment of PMM2-Congenital Disorder of Glycosylation. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG1-CDG, PMM2-Congenital Disorder of Glycosylation, Childhood Acute Myeloid Leukemia, and Leukemia.

    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
    Showing 1-13 of 13

    Last Updated: 04/28/2026

    What is the definition of PMM2-Congenital Disorder of Glycosylation?

    PMM2-congenital disorder of glycosylation (PMM2-CDG, also known as congenital disorder of glycosylation type Ia) is an inherited condition that affects many parts of the body. The type and severity of problems associated with PMM2-CDG vary widely among affected individuals, sometimes even among members of the same family.

    When should I see a PMM2-Congenital Disorder of Glycosylation doctor in Mexico?

    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 PMM2-Congenital Disorder of Glycosylation doctor in Mexico?

    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 do I find the best PMM2-Congenital Disorder of Glycosylation doctor in Mexico?

    You can find a PMM2-Congenital Disorder of Glycosylation doctor in any of the 10 largest U.S. cities by clicking below:

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    How does MediFind rank PMM2-Congenital Disorder of Glycosylation doctors in Mexico?

    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 PMM2-Congenital Disorder of Glycosylation doctors in Mexico?

    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 PMM2-Congenital Disorder of Glycosylation doctor in Mexico?

    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 PMM2-Congenital Disorder of Glycosylation doctor search results page. 

    Why is it important to get a second opinion from a different PMM2-Congenital Disorder of Glycosylation 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 PMM2-Congenital Disorder of Glycosylation doctor in Mexico?

    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 PMM2-Congenital Disorder of Glycosylation 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 PMM2-Congenital Disorder of Glycosylation 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 PMM2-Congenital Disorder of Glycosylation doctors in Mexico?

    Look for the filter feature on the left side of the PMM2-Congenital Disorder of Glycosylation 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 PMM2-Congenital Disorder of Glycosylation doctor that offers video calls?

    Look for the filter feature on the left-side of the PMM2-Congenital Disorder of Glycosylation 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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