Congenital anomalies, also known as birth defects, are structural or functional abnormalities, including metabolic disorders, that are present from birth. Congenital anomalies are a diverse group of disorders of prenatal origin that can be caused by single gene defects, chromosomal disorders, multifactorial inheritance, environmental teratogens or micronutrient malnutrition. This atlas of selected congenital anomalies is a companion tool to Birth Defects Surveillance: A Manual for Program Managers, and is intended to help in the development, implementation and ongoing improvement of a surveillance program for congenital anomalies, particularly in countries with limited human and financial resources. This atlas uses the International statistical classification of diseases and related health problems. - 10th revision, 10th revision (ICD-10) and the Royal College of Paediatrics and Child Health (RCPCH) extension for coding of congenital anomalies. This atlas provides selected illustration...
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