Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo - Ornithine - Document - PDFSEARCH.IO

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	Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo Add to Reading List Document Date: 2009-07-15 13:48:21 Open Document File Size: 458,13 KB Share Result on Facebook Facility American College of Medical Genetics / / MedicalCondition Allergy / inherited disorder / illness / Arginosuccinic Lyase Deficiency / / MedicalTreatment dialysis / / Organization American College of Medical Genetics / / / Position Physician / Metabolic Specialist / / Product Ammonul / / Technology dialysis / / URL http / SocialTag Argininosuccinic aciduria Hyperammonemia Organic acidemia Carnitine Medical genetics Medicine Health Rare diseases

Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overloAdd to Reading List