Hydroxyacyl-coa dehydrogenase, type 2, deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Some cases simply involve developmental delay. More detailed information about the symptoms, causes, and treatments of Hydroxyacyl-coa dehydrogenase, type 2, deficiency is available below.
See full list of 17 symptoms of Hydroxyacyl-coa dehydrogenase, type 2, deficiency
Read more about treatments for Hydroxyacyl-coa dehydrogenase, type 2, deficiency
Read more about causes of Hydroxyacyl-coa dehydrogenase, type 2, deficiency.
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see ...read more »
Read more about Misdiagnosis and Hydroxyacyl-coa dehydrogenase, type 2, deficiency
Types of Hydroxyacyl-coa dehydrogenase, type 2, deficiency
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