一：无过氧化氢酶血症的是什么意思（中英文）解释的意思

无过氧化氢酶血症是一种罕见的遗传性疾病，也被称为“缺乏过氧化氢酶血症”。它是由于身体缺乏一种名为过氧化氢酶的酶而引起的，这种酶在身体内起着重要的抗氧化作用。因此，患者会出现各种各样的症状，包括肌肉无力、智力发育迟缓、癫痫等。

What is the meaning of Hypohydrogenaseemia (Chinese and English) explanation:

Hypohydrogenaseemia, also known as "lack of hydrogen peroxide enzymeemia", is a rare hereditary disease. It is caused by a lack of an enzyme called hydrogen peroxide enzyme in the body, which plays an important role in antioxidant function. Therefore, patients may experience various symptoms, including muscle weakness, delayed intellectual development, epilepsy, etc.

二：怎么读（音标）

无过氧化氢酶血症：wú guò yǎng huà qīng shù xuè zhèng

Hypohydrogenaseemia: /ˌhaɪpəʊhaɪdrəʊdʒənˈeɪzimiːə/

三：用法

无过氧化氢酶血症通常用来指代一种遗传性疾病，也可以简称为“无过氧化氢酶症”。它可以作为医学术语使用，也可以作为一般性的诊断名称。在医学文献中，也会经常出现缩写形式：HHD。

Usage:

Hypohydrogenaseemia is usually used to refer to a hereditary disease, and can also be referred to as "hypohydrogenase disorder". It can be used as a medical term or a general diagnostic name. In medical literature, the abbreviation "HHD" may also appear frequently.

四：例句1-5句且中英对照

1. 无过氧化氢酶血症是一种罕见的遗传性疾病，目前尚无有效的治疗方法。

Hypohydrogenaseemia is a rare hereditary disease and there is currently no effective treatment.

2. 患者的肌肉无力可能是由于缺乏过氧化氢酶引起的。

The patient's muscle weakness may be caused by a lack of hydrogen peroxide enzyme.

3. 这种遗传性疾病会导致智力发育迟缓和其他神经问题。

This hereditary disease can lead to delayed intellectual development and other neurological problems.

4. 医生建议患者进行基因检测，以确认是否患有无过氧化氢酶血症。

Doctors recommend genetic testing for patients to confirm whether they have hypohydrogenaseemia.

5. 这种疾病也被称为“缺乏过氧化氢酶血症”，因为它是由于缺乏这种酶而引起的。

This disease is also known as "lack of hydrogen peroxide enzymeemia" because it is caused by a lack of this enzyme.

五：同义词及用法

无过氧化氢酶血症可以被称为“缺乏过氧化氢酶血症”或者“缺少过氧化氢酶血症”。在医学文献中，也会经常出现缩写形式：HHD。

Synonyms and usage:

Hypohydrogenaseemia can be referred to as "lack of hydrogen peroxide enzymeemia" or "deficiency of hydrogen peroxide enzymeemia". In medical literature, the abbreviation "HHD" may also appear frequently.

六：编辑总结

无过氧化氢酶血症是一种罕见的遗传性疾病，由于身体缺乏一种重要的抗氧化酶而引起。它可以导致各种各样的临床表现，如肌肉无力、智力发育迟缓、癫痫等。该术语可以作为医学术语使用，也可以作为一般性的诊断名称。在医学文献中，也会经常出现缩写形式：HHD。了解这一术语的含义和用法，有助于更好地理解相关的医学知识和疾病。