Gaucher disease is an inherited disorder that affects many of the body's organs and tissues. The signs and symptoms of this condition vary widely among affected ...

... in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr;112(4): ...

... in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr;112(4): ...

... diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the ...

... diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the ...

... 40 percent of those with other forms of acute myeloid leukemia. However, the disease recurs in approximately half of them after successful treatment of the initial occurrence. Acute myeloid leukemia occurs in approximately 3.5 per ...

... they cause the cutaneous forms of porphyria. The acute forms of the disease occur when porphyrins and porphyrin precursors build up ...

... KD Mucocutaneous lymph node syndrome Genetic Testing Registry: Acute febrile mucocutaneous lymph node syndrome Kawasaki disease National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...

... 1, also known as susceptibility to infection-induced acute encephalopathy 3 or IIAE3, is a rare type of brain disease (encephalopathy) that occurs following a viral infection such ...

... Most individuals with GM2 activator deficiency have the acute infantile form of the disease. Signs and symptoms of acute infantile GM2 activator deficiency typically appear between the ...