更新于:2024-11-01

Urea Cycle Disorders, Inborn

尿素循环障碍

基本信息

别名
DISORDERS OF THE UREA CYCLE METABOLISM、Disorder of the urea cycle metabolism、Disorder of the urea cycle metabolism (disorder)
+ [28]
简介
Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inactivity of an enzyme, involved in the urea cycle. Neonatal onset results in clinical features that include irritability, vomiting, lethargy, seizures, NEONATAL HYPOTONIA; RESPIRATORY ALKALOSIS; HYPERAMMONEMIA; coma, and death. Survivors of the neonatal onset and childhood/adult onset disorders share common risks for ENCEPHALOPATHIES, METABOLIC, INBORN; and RESPIRATORY ALKALOSIS due to HYPERAMMONEMIA.

分析

对领域进行一次全面的分析。
对领域进行一次全面的分析。
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