Inborn branched chain aminoaciduria
Overview
Inborn branched chain aminoaciduria: Any inherited disorder that results in abnormally high levels of branched chain amino acids in the urine. Branched chain amino acids includes leucine, valine and isoleucine. Maple syrup urine disease is the main inborn disorder that causes this form of aminoaciduria.
Symptoms
High amino acid level in urine
Diagnosis
The phrase "signs of Inborn branched chain aminoaciduria" should, strictly speaking, refer only to those signs and symptoms of Inborn branched chain aminoaciduria that are not readily apparent to the patient. The word "symptoms of Inborn branched chain aminoaciduria" is the more general meaning; see symptoms of Inborn branched chain aminoaciduria. The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Inborn branched chain aminoaciduria. This medical information about signs and symptoms for Inborn branched chain aminoaciduria has been gathered from various sources, may not be fully accurate, and may not be the full list of Inborn branched chain aminoaciduria signs or Inborn branched chain aminoaciduria symptoms. Furthermore, signs and symptoms of Inborn branched chain aminoaciduria may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Inborn branched chain aminoaciduria symptoms.