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Current understanding and progress of research on isovaleric acidemia / 中华医学遗传学杂志
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-928371
Responsible library: WPRO
ABSTRACT
Isovaleric acidemia is a type of organic acidemia for which the earliest definite diagnosis was attained. It features an autosomal recessive inheritance, with the onset of age varying from newborn to adulthood. The clinical manifestations are complex and variable, which include feeding difficulty, vomiting, lethargy, coma, metabolic acidosis, sweaty feet odor and mental retardation. The mortality and mobility rates of isovaleric acidemia are quite high, and early diagnosis and rational treatment can significantly improve the prognosis. This article has provided a summary for the current understanding and research progress on isovaleric acidemia.
Subject(s)
Full text: Available Database: WPRIM (Western Pacific) Main subject: Isovaleryl-CoA Dehydrogenase / Amino Acid Metabolism, Inborn Errors Type of study: Prognostic study / Screening study Limits: Adult / Humans / Infant, Newborn Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2022 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Isovaleryl-CoA Dehydrogenase / Amino Acid Metabolism, Inborn Errors Type of study: Prognostic study / Screening study Limits: Adult / Humans / Infant, Newborn Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2022 Document type: Article
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