Study on genetic diagnosis and prenatal diagnosis of alpha-thalassemia.
- Author:
Jing-zhong LIU
1
;
Li-rong WANG
;
Li-jia HUANG
;
Bai XIAO
;
Yan ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Child, Preschool; Family Health; Female; Fetal Diseases; diagnosis; genetics; Gene Deletion; Genetic Testing; Humans; Male; Molecular Diagnostic Techniques; methods; Point Mutation; Polymerase Chain Reaction; methods; Pregnancy; Prenatal Diagnosis; Sequence Analysis, DNA; alpha-Thalassemia; diagnosis; genetics
- From: Chinese Journal of Hematology 2005;26(2):103-105
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo develop a single-tube multiplex polymerase chain reaction (mPCR) technique to detect three common deletional alpha-thalassemias (alpha-Thal) in Chinese, and to perform genetic diagnosis and prenatal diagnosis for an alpha-Thal family from Hebei province, China.
METHODSFourty-two blood samples including samples from one alpha-Thal family from Hebei province were assayed. The mPCR containing 7 primers, gel electrophoresis and DNA sequencing were used for the genetic diagnosis and prenatal diagnosis.
RESULTSThe gene types of the fourty-two DNA samples analyzed by the mPCR-gel electrophoresis technique were in accordance with the results by Southern blot and three separate PCR techniques. A HbH child and a fetus of the alpha-Thal family were diagnosed as--(SEA)/alpha(cs)alpha and alpha alpha/alpha alpha respectively by using the mPCR and DNA sequencing. The result of postnatal analysis of the cord blood was consistent with the prenatal result (alpha alpha/alpha alpha).
CONCLUSIONThe developed mPCR technique can be used for genetic diagnosis and prenatal diagnosis of the 3 deletional alpha-Thal in Chinese.