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Progressive Liver Fibrosis in Late-onset Argininosuccinate Lyase Deficiency

โœ Scribed by Toshihiko Mori; Kazushige Nagai; Michio Mori; Masayoshi Nagao; Masakatsu Imamura; Mikio Iijima; Keiko Kobayashi


Book ID
106249450
Publisher
Springer
Year
2002
Tongue
English
Weight
982 KB
Volume
5
Category
Article
ISSN
1093-5266

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Urea cycle disorders (UCDs) are rare causes of hyperammonemic encephalopathy in adults. Most UCDs present in childhood and, if unrecognized, are rapidly fatal. Affected individuals who survive to adulthood may remain undiagnosed because of clinicians' unawareness of the condition or atypical present