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Methylmalonic Acidemia CblA Type
A methylmalonic acidemia characterized by autosomal recessive inheritance, defects in the synthesis of AdoCbl, vitamin B12 therapy responsiveness and that is caused by homozygous or compound heterozygous mutation in the
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Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A methylmalonic acidemia characterized by autosomal recessive inheritance, defects in the synthesis of AdoCbl, vitamin B12 therapy responsiveness and that is caused by homozygous or compound heterozygous mutation in the
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.