epidermolysis

简明释义

英[epɪdəˈmɒləsɪs]美[epɪdərˈmɔːləsɪs]

n. [医] 表皮松解

英英释义

单词用法

同义词

反义词

例句

1.Conclusions The splicing mutation of COL7A1 gene is the underlying cause of and specific rather than common polymorphism for the family with dystrophic epidermolysis bullosa pruriginosa subtype.

结论COL7A1基因剪接位点的突变是引起该家系临床症状的特异突变，而非多态性改变。

2.Conclusions The splicing mutation of COL7A1 gene is the underlying cause of and specific rather than common polymorphism for the family with dystrophic epidermolysis bullosa pruriginosa subtype.

结论COL7A1基因剪接位点的突变是引起该家系临床症状的特异突变，而非多态性改变。

3.Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.

一种遗传疾病，以先天性局部皮肤缺损、大疱性表皮松解症、口腔粘膜病变、甲营养不良为特征。

4.Objective to investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.

目的总结中毒性表皮松解症(TEN)患者的护理经验，提高护理质量，有效地促进患者康复。

5.Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.

目的：通过透射电镜和免疫荧光研究先天性大疱性表皮松解症患者的基底膜带分子。

6.Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.

儿童获得性大疱表皮松解症（EBA）是一种自身免疫性表皮下大疱病，比较少见。

7.Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.

前期的临床实验在治疗创伤，大疱性表皮松解症和鱼鳞病上已经取得了进展。

8.Objective: Analysis characteristic and regularity of epidermolysis bullosa type eruption.

目的：探讨大疱性表皮松解型药疹的发生特点及一般规律。

9.The patient was diagnosed with epidermolysis, a condition that causes the skin to be extremely fragile.

患者被诊断为表皮松解症，一种导致皮肤极其脆弱的病症。

10.In severe cases of epidermolysis, even minor friction can lead to painful blisters.

在严重的表皮松解症情况下，即使是轻微的摩擦也会导致疼痛的水泡。

11.Treatment for epidermolysis often involves specialized bandaging to protect the skin.

治疗表皮松解症通常需要特殊的绷带来保护皮肤。

12.Research is ongoing to find a genetic cure for epidermolysis.

针对表皮松解症的基因治疗研究仍在进行中。

13.Children with epidermolysis require extra care to avoid skin injuries.

患有表皮松解症的儿童需要额外的护理，以避免皮肤受伤。

作文

Epidermolysis is a term that refers to a rare group of genetic skin disorders characterized by the fragility of the skin. Individuals affected by this condition experience severe blistering and tearing of the skin, often with minimal friction or trauma. The skin's outer layer, known as the epidermis, separates from the underlying layers, leading to painful sores and an increased risk of infection. This condition can significantly affect the quality of life for those who suffer from it, as daily activities can become challenging due to the sensitivity of their skin. Understanding epidermolysis (表皮松解症) requires knowledge of the various types that exist. The most common type is Epidermolysis Bullosa (EB), which is further classified into several subtypes based on the specific genetic mutations involved. Each subtype presents different symptoms and levels of severity. For example, some individuals may develop blisters only on their hands and feet, while others may experience widespread blistering across their entire body. The cause of epidermolysis (表皮松解症) lies in mutations of genes responsible for the production of proteins that help anchor the epidermis to the dermis, the layer of skin underneath. These mutations disrupt the structural integrity of the skin, making it more susceptible to damage. Research has shown that the condition can be inherited in an autosomal dominant or recessive manner, depending on the specific type of EB. Living with epidermolysis (表皮松解症) can be incredibly challenging. Patients must take extra precautions to protect their skin, such as wearing soft clothing, avoiding extreme temperatures, and maintaining good hygiene to prevent infections. Treatment options are limited, but they often focus on wound care, pain management, and preventing complications. In some cases, patients may benefit from physical therapy to maintain mobility and strength, especially if they have developed contractures due to scarring. Research into epidermolysis (表皮松解症) is ongoing, with scientists exploring gene therapy as a potential treatment option. By correcting the genetic mutations that cause the condition, there is hope for more effective treatments in the future. Additionally, support groups and organizations play a crucial role in providing resources and community for affected individuals and their families. These groups advocate for awareness and research funding, aiming to improve the lives of those impacted by this debilitating condition. In conclusion, epidermolysis (表皮松解症) is a complex and challenging condition that requires a multifaceted approach to management and treatment. Awareness and understanding of this disorder are essential not only for those affected but also for healthcare providers and the general public. By fostering a supportive environment and promoting research, we can hope for advancements that will lead to better outcomes for individuals living with this condition.