分子病検査診断「症例呈示と病態解析」(1)

分子病検査診断

安　東　由喜雄*
　　　　　　　　　　　　　　　　　　　　　　
Novel Procedures for Diagnosis of Genetic Metabolic Disorders

Yukio ANDO, MD*

Owing to the progress of molecular genetics, various methodologies have been applied to routine works in Laboratory Medicine and contribute the discovery of new diseases and physicochemical analyses. It is very important to be up-to-date on new methodologies which may be useful in diagnosis of common diseases as well as genetic metabolic disorders. In this symposium, 5 well-known speakers introduced novel diagnostic methods, and presented novel data on physico-chemical aspects of amyloidosis, hereditary neuropathies, hemoglobin disorders, hereditary diabetes mellitus, and thalathemia based on molecular and biochemical approaches.
[Rinsho Byori 51 : 528〜529, 2003]

*Department of Laboratory Medicine, Kumamoto University School of Medicine, Kumamoto 860-8556

【Key Words】amyloidosis hereditary neuropathy(遺伝性アミロイドーシス)，hemoglobin disorders(異常ヘモグロビン)，diabetes mellitus(糖尿病)，thalathemia(サラセミア)

*熊本大学医学部臨床検査医学(〒860-8556 熊本市本荘1-1-1)

E-mail :yukio@kaiju.medic.kumamoto-u.ac.jp