It's very difficult to treat genetic diseases.

性疾病治疗起来很困难。

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

目的分析儿童性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.

研究性白内障致病因，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，患有性语言障碍（verbaldyspraxia）的一家人引起了因学者的注意。

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

甲酸血症是由于甲酰辅A变位或其辅腺苷钴胺素缺陷所致的一性代谢疾病。

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

先天性角化不良症（DKC）为一少见之性疾病，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-性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.

阐述了性、下丘脑性及饮食诱导性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性掌跖皮肤角化病—性残毁性角化瘤,并与各掌跖皮肤角化症、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.

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

It's very difficult to treat genetic diseases.

遗疾病治疗起来很困难。

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

目的分析儿童遗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.

研究遗白内障致病因，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，患有遗语言障碍（verbaldyspraxia）的一家人引起了因学者的注。

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

丙二酸血症是由于丙二酰辅A变位或其辅腺苷钴胺素缺陷所致的一种遗谢疾病。

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）为一少见之遗疾病，三项主要特徵为皮肤色素异常、 指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-遗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.

阐述了遗、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遗掌跖皮肤角化病—遗残毁角化瘤,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、风害及遗白化症等，以及病因不明之尾叶桉皱叶病亦在文内叙述之。

It's very difficult to treat genetic diseases.

遗传性疾病治疗起来很困难。

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

目的分析儿童遗传性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.

研究遗传性白内障致病基因，实验型是一个非好的方式。

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

1990年，患有遗传性语言障碍（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.

基丙二酸血症是由于基丙二酰辅A变位或其辅腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

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

先天性角化不良症（DKC）为一少见之遗传性疾病，三项主要特徵为皮肤色素异、 生长异及黏膜白斑症。

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-遗传性疾病与异运和心理的恶化'?

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

阐述了遗传性、下丘脑性及饮食诱导性肥胖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遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,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.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害及遗传性白化症等，以及病因不明之尾叶桉皱叶病亦在文内叙述之。

It's very difficult to treat genetic diseases.

遗传性疾病治疗起来很困难。

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

目的分析儿童遗传性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.

研究遗传性病基因，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，患有遗传性语言碍（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的一种遗传性代谢疾病。

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

先天性角化不良症（DKC）为一少见之遗传性疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及斑症。

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-遗传性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.

阐述了遗传性、下丘脑性及饮食诱导性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遗传性掌跖皮肤角化病—遗传性残毁性角化瘤,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.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害及遗传性化症等，以及病因不明之尾叶桉皱叶病亦在文叙述之。

It's very difficult to treat genetic diseases.

遗传治疗起来很困难。

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

目的分析儿童遗传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.

研究遗传白内障致基因，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，患有遗传语言障碍（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遗传代谢。

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）为一少见之遗传，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-遗传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.

阐述了遗传、下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遗传掌跖皮肤角化—遗传残毁角化瘤,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.

此外非原害包括红斑、流胶、除草剂药害、风害及遗传白化症等，以及因不明之尾叶桉皱叶亦在文内叙述之。

It's very difficult to treat genetic diseases.

遗传疾病治疗来很困难。

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

目的分析儿童遗传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.

研究遗传白内障致病因，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，患有遗传语言障碍（verbaldyspraxia）的一家人引因学者的注意。

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

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

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

先天不良症（DKC）为一少见之遗传疾病，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-遗传疾病与异常运动和心理的恶'?

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

阐述遗传、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.

本文报告一例罕见的遗传掌跖皮肤病—遗传残毁瘤,并与各种掌跖皮肤症、断肢症的鉴别进行讨论。

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、风害及遗传白症等，以及病因不明之尾叶桉皱叶病亦在文内叙述之。

It's very difficult to treat genetic diseases.

传性疾病治疗起难。

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

目的分析儿童传性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.

研究传性白内障致病基因，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，患有传性语言障碍（verbaldyspraxia）的一家人引起基因学者的注意。

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传性代谢疾病。

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

先天性角化不良症（DKC）为一少见之传性疾病，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-传性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.

阐传性、下丘脑性及饮食诱导性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.

本文报告一例罕见的传性掌跖皮肤角化病—传性残毁性角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行讨论。

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.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害及传性白化症等，以及病因不明之尾叶桉皱叶病亦在文内叙之。

It's very difficult to treat genetic diseases.

性疾病治疗起来很困难。

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

目的分析儿童性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.

研究性白内障致病基因，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，患有性语言障碍（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性代谢疾病。

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

先天性角化不良症（DKC）为一少见之性疾病，三项主要特徵为皮肤色素异常、 指甲生长异常黏膜白斑症。

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-性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.

阐述了性、下丘脑性诱导性肥胖动物模型的造型方法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性掌跖皮肤角化病—性残毁性角化瘤,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.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害性白化症等，以病因不明之尾叶桉皱叶病亦在文内叙述之。

It's very difficult to treat genetic diseases.

传性疾病治疗起来很困难。

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

目的分析儿童传性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.

研究传性白内障致病基因，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，患有传性语言障碍（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传性代谢疾病。

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

先天性角化不良症（DKC）为一少见之传性疾病，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-传性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.

阐述了传性、下丘脑性及导性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传性掌跖皮肤角化病—传性残毁性角化瘤,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.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害及传性白化症等，以及病因不明之尾叶桉皱叶病亦在文内叙述之。