D-glyceric aciduria

A metabolic disorder characterized by D-glyceric acid excretion. It has been described in several patients. Clinical findings include progressive neurological impairment, hypotonia, seizures, failure to thrive and metabolic acidosis. Some patients had hyperglycinemia secondary to the organic acidemia. However, some of the reported patients were asymptomatic. D-glyceric aciduria is caused by D-glycerate kinase deficiency. The GLYCTK gene has been mapped to 3p21.

Also known as: D-glycerate kinase deficiency, D-glyceric acidemia, d-glyceric aciduria, D-glycericacidemia, glycerate kinase deficiency, non ketotic hyperglycinemia syndrome

0 clinical trials for this condition and its sub-types.