遗传性

It's very difficult to treat genetic diseases.

疾病治疗起来很困难。

Objective To analyze the clinical feature of children hereditary spherocytosis (HS).

目的分析儿童球形红细胞增多症的临床特点。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究白内障致病基因，实验动物模型是一个非常好的方式。

In 1990, a family with an inherited speech disorder known as verbal dyspraxia drew the attention of genetics researchers.

1990年，患有语障碍（verbaldyspraxia）的一家人引起了基因学者的注意。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅A变位或其辅腺苷钴胺素缺陷所致的一种代谢疾病。

Dyskeratosis congenita (DKC) is a rare inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy, and mucosal leukoplakia.

先天角化不良症（DKC）为一少见疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

HD is caused by a trinucleotide repeat expansion in the Huntingtin (Htt) gene; and is one of several polyglutamine (or PolyQ) diseases.

什么是'少年亨廷顿疾病-疾病与异常运动和心理的恶化'?

In this paper are elaborated the methods of induced obesity by hereditation ,hypothalamic lesions and dietary in experimental animals,and the concerned physiological characteristics.

阐述了、下丘脑及饮食诱导肥胖动物模型的造型方法及有关的生理代谢特点.

This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的掌跖皮肤角化病—残毁角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。

Several non-infectious diseases including the leaf red spot, gummosis, herbicide in jury, typhoon damage and genetic albinism and an unidentified leaf crinkle disease are also described.

此外非病原病害包括红斑病、流胶病、除草剂药害、风害及白化症等，以及病因不明尾叶桉皱叶病亦在文内叙述。