hereditary diseases

How Are Hereditary Diseases Diagnosed?

Diagnosis of hereditary diseases typically involves a combination of:
- Family History: Collecting detailed family medical histories to identify patterns.
- Genetic Testing: Using techniques like Polymerase Chain Reaction (PCR) and Next-Generation Sequencing to detect genetic mutations.
- Clinical Evaluation: Assessing symptoms and using imaging studies and biochemical tests to identify clinical manifestations of genetic disorders.

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