See what questions
a doctor would ask.
Glycine synthase deficiency, type 2: A rare genetic disorder characterized by high blood glycine levels. It is caused by a defect in the T protein (tetrahydrofolate-requiring enzyme) in the energy creating center of cells (mitochondria). More detailed information about the symptoms, causes, and treatments of Glycine synthase deficiency, type 2 is available below.
Read more about causes of Glycine synthase deficiency, type 2.
Research the causes of these diseases that are similar to, or related to, Glycine synthase deficiency, type 2:
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12...read more »
Read about other experiences, ask a question about Glycine synthase deficiency, type 2, or answer someone else's question, on our message boards:
Search Specialists by State and City