Your browser doesn't support javascript.
loading
Prenatal diagnosis down syndrome, turner syndrome by using fluorescence in situ hybridization (FISH) technique with chromosome analysis from amniotic cell
Article de Vi | WPRIM | ID: wpr-332
Bibliothèque responsable: WPRO
ABSTRACT
Background: FISH can detect number and structural chromosome aberrations in DNA. FISH is new technique in Vietnam, we combine FISH with chromosome analysis to prenatal diagnosis Down syndrome and turner syndrome that are high rate in birth defect.Objectives: To detect Down syndrome and turner syndrome by using FISH technique with chromosome analysis from amniotic cell.Subjects and method: 14amniotic cells samples 15th - 20th week with high risk of birth defects. Advance using FISH and chromosome analysis from amniotic cell. Results: We obtained results as follow: - 14/14 samples: correspondence between FISH and chromosome analysis. \ufffd?Detected 2 Down syndrome (female. Trisomi 21) and 4 Turner syndrome (45, X). Conclusion: Detected Down syndrome and Turner syndrome by using FISH technique with chromosome analysis from amniotic cell.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Diagnostic prénatal / Syndrome de Turner / Valeur prédictive des tests / Hybridation in situ / Syndrome de Down / Fluorescence Type d'étude: Diagnostic_studies / Prognostic_studies langue: Vi Texte intégral: Journal of Medical Research Année: 2007 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Diagnostic prénatal / Syndrome de Turner / Valeur prédictive des tests / Hybridation in situ / Syndrome de Down / Fluorescence Type d'étude: Diagnostic_studies / Prognostic_studies langue: Vi Texte intégral: Journal of Medical Research Année: 2007 Type: Article