Click to see the original definition of «크산틴뇨증» in the Korean dictionary.
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Definition of 크산틴뇨증 in the Korean dictionary
Xanthinuria Hereditary is the purine metabolism abnormality (metabolic abnormality) caused by genetic deficiency of xanthine oxidase (XO). Increased xanthine (X) and hypoxanthin (HX) in blood and urine (urine), and uric acid is decreased markedly. Symptoms are not necessarily accompanied. 크산틴뇨증 유전성인 것은 크산틴산화효소(XO)의 유전적 결손에 의하여 일어나는 푸린체대사이상(代謝異常). 혈액ㆍ요중(尿中)에 크산틴(X)ㆍ히포크산틴(HX)이 증가하고 요산이 뚜렷이 감소. 증상은 반드시 수반되지는 않는다.
Click to see the original definition of «크산틴뇨증» in the Korean dictionary.
Click to see the automatic translation of the definition in English.
The translations of 크산틴뇨증 from Korean to other languages presented in this section have been obtained through automatic statistical translation; where the essential translation unit is the word «크산틴뇨증» in Korean.
The map shown above gives the frequency of use of the term «크산틴뇨증» in the different countries.
Examples of use in the Korean literature, quotes and news about 크산틴뇨증
EXAMPLES
KOREAN BOOKS RELATING TO «크산틴뇨증»
Discover the use of 크산틴뇨증 in the following bibliographical selection. Books relating to 크산틴뇨증 and brief extracts from same to provide context of its use in Korean literature.
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중증 장애인의 교육과 재활: - 62페이지
정신 지체 를 유발 하는 이 유형 의 질환 은 선천성 크 레틴 병 ( congenitalcretinisrn ) , 갑상선 성 크레 틴병 ( goi ... 정신 지체 를 유발 하는 뉴클레오티드 장애 는 산 뇨증 ( iiciduria ) , 잔틴 뇨증 ( Xan ( hinuro , 요산 과다 혈증 ( hyperurkernia ) 등 이다 .
리처드 W.브라이머, 1996
REFERENCE
« EDUCALINGO. 크산틴뇨증 [online]. Available <https://educalingo.com/en/dic-ko/keusantinnyojeung>. May 2024 ».