?a-k?-tal-?-?zē-mē

noun

A rare genetic disorder characterized by a deficiency of the enzyme catalase.

一個罕見的遺傳性疾病，其特征是缺乏酶催化劑。

例句1：Acatalasemia is an inherited disorder that affects the body's ability to break down hydrogen peroxide.

acatalasemia是一種遺傳性疾病，它會影響身體分解過氧化氫的能力。

例句2：People with acatalasemia may experience symptoms such as oral ulcers, skin lesions, and an increased risk of infections.

患有acatalasemia的人可能會出現(xiàn)口腔潰瘍、皮膚損傷和感染風險增加等癥狀。

例句3：The diagnosis of acatalasemia is usually made through genetic testing and a physical examination.

通常通過基因測試和體格檢查來診斷acatalasemia。

例句4：There is currently no cure for acatalasemia, but treatments such as vitamin supplements can help manage symptoms.

目前尚無治愈acatalasemia的方法，但補充維生素等治療可以幫助癥狀。

例句5：Individuals with acatalasemia should avoid exposure to certain chemicals and medications that can worsen their condition.

患有acatalasemia的人應避免接觸某些化學物質(zhì)和藥物，這些物質(zhì)可能會加重他們的病情。

同義詞及用法：

1. Catalase deficiency: This is another term used to describe the condition of acatalasemia, as it is caused by a deficiency of the enzyme catalase.

酶催化劑缺乏癥：這是另一個用來描述acatalasemia狀況的術(shù)語，因為它是由酶催化劑缺乏引起的。

2. Hydrogen peroxide disorder: This term refers to the inability of the body to break down hydrogen peroxide, which is a characteristic feature of acatalasemia.

過氧化氫疾?。哼@個術(shù)語指的是身體無法分解過氧化氫，這是acatalasemia的典型特征。

3. Peroxisomal disorder: Acatalasemia is considered a peroxisomal disorder, as it affects the functioning of peroxisomes, which are cellular organelles responsible for breaking down hydrogen peroxide.

過氧化物體失調(diào)：acatalasemia被認為是一種過氧化物體失調(diào)，因為它影響了過氧化物體的功能，而過氧化物體是負責分解過氧化氫的細胞器。

編輯總結(jié)：

Acatalasemia是一種罕見的遺傳性疾病，其特征是缺乏酶催化劑。它可以通過基因測試和體格檢查來診斷，并且目前尚無治愈方法，但可以通過補充維生素等治療來癥狀。同義詞包括Catalase deficiency、Hydrogen peroxide disorder和Peroxisomal disorder。了解這個單詞的意思和用法可以幫助我們更好地理解這種罕見的遺傳性疾病。