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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency : ウィキペディア英語版 | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OH CAH), in all its forms, accounts for over 95% of diagnosed cases of congenital adrenal hyperplasia, and "CAH" in most contexts refers to 21-hydroxylase deficiency. An overview of the other types of CAH is presented in the main article. ==Degree of severity== The condition can be classified into "salt-wasting", "simple virilizing", and "non-classical" forms. The salt-wasting and simple virilizing types are sometimes grouped together as "classical".
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Congenital adrenal hyperplasia due to 21-hydroxylase deficiency」の詳細全文を読む
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