Congenital anomalies

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Congenital anomalies

Congenital anomalies (pronunciation: /kənˈjenɪtl ˈænəˌmɑːlɪz/), also known as birth defects, are structural or functional anomalies, including metabolic disorders, which are present at the time of birth.

Etymology

The term "congenital" is derived from Latin congenitus, which means "born with" or "existing from birth". "Anomaly" comes from the Greek word anomalía meaning "irregularity" or "deviation".

Definition

Congenital anomalies are a diverse group of disorders of prenatal origin which can be caused by single gene defects, chromosomal disorders, multifactorial inheritance, environmental teratogens and micronutrient deficiencies.

Classification

Congenital anomalies can be classified into two main types: structural anomalies and functional anomalies.

Causes

The causes of congenital anomalies can be genetic, environmental, or unknown.

  • Genetic causes include single gene defects, chromosomal disorders, and multifactorial inheritance.
  • Environmental causes include exposure to certain drugs, chemicals, or infections during pregnancy, which can act as teratogens.
  • In many cases, the cause of the congenital anomaly is unknown.

Prevention and Management

Prevention of congenital anomalies includes the control of infectious diseases in the mother, improving maternal nutrition, avoiding exposure to harmful environmental factors, and genetic counseling. Management of congenital anomalies depends on the specific condition and may include surgical intervention, medical treatment, and physical therapy.

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