Ehlers-Danlos syndrome
People with Ehlers-Danlos have very loose joints and easily bruised or stretchy skin. Symptoms can be managed, but there is a higher risk of injury.
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Family health history
Knowing your family medical history is important. It can guide you in making changes that will reduce your risk of developing a hereditary condition.
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Apert syndrome
Apert syndrome is a rare genetic disorder that causes changes to the shape of the skull. Learn more about the other signs of Apert syndrome.
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Tay-Sachs disease
Babies with Tay-Sachs develop slowly, lose vision and speech and typically don't reach school age. It's more common in certain genetic groups.
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Genetic testing
Genetic testing can give you information if you're planning a family, or if you or your partner has a genetic disorder. Learn when counselling can help.
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Guide to genetic disorders
Genetic issues impact many aspects of health and development. Some affect people from birth, while others develop later in life. Read on for details.
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Huntington's disease
Huntington's affects the nervous system and worsens over time. Symptoms include difficulty controlling limbs and cognitive and emotional changes.
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Rett syndrome
Rett syndrome causes intellectual and physical disability. It’s been described relatively recently, so it’s not known how it progresses to middle age.
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Lynch syndrome
Lynch syndrome, formerly known as HNPCC, is a genetic condition that increases the risk of a person developing some cancers, such as bowel cancer.
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Tuberous sclerosis
Tuberous sclerosis is a rare genetic disease that may affect many parts of your body, behaviour and thinking. There’s no cure, but it can be treated.
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