Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2 / 中华医学遗传学杂志
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; (6): 325-328, 2004.
Article
в Zh
| WPRIM
| ID: wpr-328885
Ответственная библиотека:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To use microsatellite DNA tightly linked to polycystic kidney disease gene 2 in the gene diagnosis of autosomal dominant polycystic kidney disease type 2.</p><p><b>METHODS</b>Microsatellite DNA of D4S1534, D4S1542, D4S1563,D4S2460 and D4S423 were amplified with PCR and the fragments of products were analyzed by capillary electrophoresis and Genescan and Genotyper software, and then gene diagnosis of the pedigrees was made by linkage analysis.</p><p><b>RESULTS</b>Three families were found to be linked to PKD2 in 20 families. Two carriers of PKD2 mutation were revealed by linkage analysis.</p><p><b>CONCLUSION</b>Gene diagnosis can be done for PKD2 mutation carriers prior to cytogenesis. Linkage analysis is a rapid, simple method for studying the heterogeneity of polycystic kidney disease and for diagnosing the disease at the molecular level.</p>
Полный текст:
1
База данных:
WPRIM
Основная тема:
Polycystic Kidney, Autosomal Dominant
/
Microsatellite Repeats
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Diagnosis
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TRPP Cation Channels
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Genetics
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Genetic Linkage
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Mutation
Тип исследования:
Diagnostic_studies
Пределы темы:
Female
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Humans
/
Male
Язык:
Zh
Журнал:
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
Год:
2004
Тип:
Article