
SINGLE-NUCLEOTIDE POLYMORPHISMS IN EXONIC
AND PROMOTER REGIONS OF TRANSCRIPTION
FACTORS OF SECOND HEART FIELD ASSOCIATED
WITH SPORADIC CONGENITAL CARDIAC ANOMALIES Wang E, Fan X, Nie Y, Zheng Z, Hu S, *Corresponding Author: Shengshou Hu M. D., Cardiac Surgery Department, Fuwai Hospital, Chinese
Academy of Medical Sciences, Peking Union Medical College, Xicheng District, Beijing, 100037,
China, Tel & Fax: 86-010-88322325 E-mail: shengshouh@sina.cn page: 39
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METHODS
Diagnosis criteria: According to the most accepted
and unified classification, Congenital Heart Surgery
Nomenclature and Database Project, the diagnosis of
VSD (1), ASD (2), PDA (3), TOF (4), PA, PS,(5) or SV(6)
were made mainly based on echocardiography. Inclusion
criteria: Patients who were younger than 18 years and
diagnosed as VSD, ASD, PDA, TOF, PA, PS or SV were
included in this study. Exclusion criteria: the subject exclusion
criteria included a family history of CHD in a firstdegree
relative (parents, siblings, or children), structural
malformations involving another organ system or known
chromosomal abnormalities, maternal DM, phenylketonuria,
maternal exposure to teratogens (e.g., pesticides and
organic solvents), and rubella, influenza, and febrile illnesses
during pregnancy.
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