Congenital anomalies

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Congenital anomalies are also known as birth defects, congenital disorders or congenital malformations. Congenital anomalies can be defined as structural or functional anomalies (e.g. metabolic disorders) that occur during intrauterine life and can be identified prenatally, at birth or later in life. Congenital anomalies can be caused by single gene defects, chromosomal disorders, multifactorial inheritance, environmental teratogens and micronutrient deficiencies.

Source: http://www.who.int/topics/congenital_anomalies/en/

Disclaimer: The above information has been taken from WHO website. Medlife is permitted to re-share WHO content in official blog and website.

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