Hereditary diseases, also known as genetic disorders, are inherited
defects that prevents an organ or tissues from working properly. These genetic mutations can be inherited from one or both parents, and they may affect various aspects of health and development.
How are they transmitted?
Hereditary diseases are transmitted through the passing of genetic
information from parents to offspring. These diseases result from mutations or abnormalities in the DNA.
How to control and treat?
For controlling and treating hereditary diseases, early detection
and management are key. Regular medical check-ups, genetic counselling, and, if available, genetic testing can help identify risks and plan preventive measures. Follow prescribed treatment plans, including medications, lifestyle modifications, and regular monitoring. Additionally, adopting a healthy lifestyle can positively impact overall health and contribute to managing the effects of hereditary diseases. Some examples of hereditary diseases are:
• Dwarfism - Dwarfism is a condition characterized by
significantly shorter stature than average for an individual's age and population group, often resulting from genetic or medical factors.
• Haemophilia - Haemophilia is a genetic disorder that impairs
the blood's ability to clot, leading to prolonged bleeding and difficulty in stopping bleeding after an injury.
• Sickle cell anaemia - Sickle cell anaemia is a genetic blood
disorder where red blood cells have a distorted, sickle-like shape, causing them to break down more easily and leading to a shortage of healthy red blood cells.
• Cystic fibrosis - Cystic fibrosis is a genetic disorder that
affects the lungs and digestive system, causing the production of thick and sticky mucus, leading to respiratory and digestive challenges.