We encourage you to consult with your healthcare provider for more information about management of lactate dehydrogenase A deficiency. A professional staff member through a Muscular Dystrophy Association (MDA) clinic can also help you design a specific plan suited for your metabolic disorder and individual needs.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
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How common is lactate dehydrogenase A deficiency and how might this condition be managed (for instance, should complex carbohydrates be avoided)?