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单词 Tuberous sclerosis
释义

Tuberous sclerosis

原声例句
Osmosis-神经

Treatment of tuberous sclerosis is focused on symptoms.

结节性硬化症的治疗主要在于对症治疗。

Osmosis-神经

Individuals with tuberous sclerosis can develop renal tumors called angiomyolipomas.

结节性硬化症可发展为肾肿瘤,称为血管平滑肌脂肪瘤。

Osmosis-神经

On top of that the lifetime risk of cancer is increased in individuals with tuberous sclerosis.

除此之外,结节性硬化症患者一生中患癌症的风险也会增加。

Osmosis-神经

Individuals with tuberous sclerosis have a mutation in either the gene TSC1 or TSC2, and these mutations have an autosomal dominant inheritance pattern.

结节性硬化症患者的TSC1或TSC2基因发生了突变,为常染色体显性遗传。

Osmosis-神经

Symptoms of tuberous sclerosis are often related to the hamartomas in the brain which cause problems like seizures, learning difficulties, and cognitive deficits.

结节性硬化症的症状通常与大脑中的错构瘤有关,导致癫痫、学习困难、认知障碍等。

Osmosis-心血管

These developmental masses happen frequently in patients that also have tuberous sclerosis —a genetic disorder causing these non-cancerous masses to form in various tissues.

这些肿块通常发生在患有结节性硬化病患者身上;结节性硬化病是一种各类组织中形成非恶性肿瘤的遗传病。

中文百科

结节性硬化症

结节性硬化症tuberous sclerosis complexTSC)是一种罕见的多系统先天性疾病,会在脑部、心脏、肾脏、皮肤及其他器官出现良性肿瘤,因此病患可能出现癫痫、发育迟缓或者脸上皮脂腺瘤等症状。 研究显示,雷帕霉素对于结节性硬化症具疗效。 数个研究确定性指出mTOR抑制剂可缓解结节性硬化症,特别是儿童的室管膜下巨细胞星形细胞瘤及成人的血管平滑肌脂肪瘤。美国在进行许多涉及结节性硬化症的雷帕霉素类似物儿童及成人临床试验。

大多数研究已注意到停止治疗后肿瘤将会复发。理论上来说,它可改善如面部血管纤维瘤、儿童多动症及自闭症等结节性硬化症症状,但这些研究还处于动物试验阶段。

英语百科

Tuberous sclerosis 结节性硬化症

Tuberous sclerosis in MRI
Computed tomography showing multiple angiomyolipomas of the kidney in a patient with lung lymphangioleiomyomatosis on CT: suspected tuberous sclerosis
The frequency of signs in children with tuberous sclerosis, grouped by age[8]

Tuberous sclerosis (also known as tuberous sclerosis complex [TSC]) is a rare multisystem genetic disease that causes benign tumors to grow in the brain and on other vital organs such as the kidneys, heart, eyes, lungs, and skin. A combination of symptoms may include seizures, intellectual disability, developmental delay, behavioral problems, skin abnormalities, and lung and kidney disease. TSC is caused by a mutation of either of two genes, TSC1 and TSC2, which code for the proteins hamartin and tuberin, respectively. These proteins act as tumor growth suppressors, agents that regulate cell proliferation and differentiation.

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更新时间:2025/6/22 23:11:21