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Prenat Diagn. 2013 Sep;33(9):869-72. doi: 10.1002/pd.4149. Epub 2013 May 21.

Prenatal control of nondeletional α-thalassemia: first experience in mainland China.

Author information

1
Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, China.

Abstract

OBJECTIVE:

To demonstrate the performance of nondeletional α-thalassemia prevention at a mainland Chinese hospital.

METHODS:

A prenatal control program for nondeletional hemoglobin H (Hb H) disease was conducted from January 2010 to June 2012. All couples were screened for α-thalassemia trait, and for couples in whom one partner was tested positive for α(0) -thalassemia, the other was subjected to screening for Hb Constant Spring and Hb Quong Sze mutations. Prenatal diagnoses were offered in pregnancies of couples at-risk for nondeletional Hb H disease.

RESULTS:

Of the 30,152 couples screened, 18 (0.06%) were diagnosed as at risk for nondeletional Hb H disease. There were other 13 at-risk couples who were referred to prenatal diagnosis because they had previously an affected child. Of the 31 cases with prenatal invasive tests, 11 (35.5%) had diagnosis by chorionic villous sampling, and 20 (64.5%) had amniocentesis. Totally, 12 fetuses were diagnosed with nondeletional Hb H disease, and all of the affected pregnancies were terminated.

CONCLUSION:

Implementation of a prevention and control program accompanying with a referral system for prenatal diagnosis is technically feasible in southern China, and a number of nondeletional Hb H disease have been prevented during the past 3 years of operation.

PMID:
23637094
DOI:
10.1002/pd.4149
[Indexed for MEDLINE]

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