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Urea cycle disorder—argininosuccinic lyase deficiency
Author(s) -
Mehta Neeta,
Kirk Pia Chatterjee,
Holder Ray,
Precheur Harry V.
Publication year - 2012
Publication title -
special care in dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.328
H-Index - 41
eISSN - 1754-4505
pISSN - 0275-1879
DOI - 10.1111/j.1754-4505.2012.00263.x
Subject(s) - medicine , urea cycle , urea , biochemistry , biology , amino acid , arginine
An increased level of ammonia in the bloodstream, or hyperammonemia, is a symptom associated with metabolic disorders referred to as inborn errors of metabolism. Urea cycle disorder is a congenital abnormality or absence of one of the six enzymes involved in the elimination of ammonia. Administration of certain medications, high protein diet, excessive exercise, surgical procedures, or trauma can precipitate symptoms of mental confusion, seizure‐like activity, and ataxia. This paper reviews the literature with insight into current treatment and management options of the disorder and modification of treatment for the dental patient.