Ehlers-Danlos syndrome
People with Ehlers-Danlos have very loose joints and easily bruised or stretchy skin. Symptoms can be managed, but the risk of injury is increased.
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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. Learn more here.
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Tay-Sachs disease
Babies/children with Tay-Sachs develop slowly, lose vision and speech, and typically don’t reach school age. It’s commoner in certain genetic groups.
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Apert syndrome
Apert syndrome is a rare condition that causes an abnormally shaped skull and fused fingers and toes. Other body parts and organs are also affected. Surgery and other treatments can, however, help development.
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Obesity at conception linked to pregnancy complications
Women should lose weight before getting pregnant if they're obese or overweight, experts say, as excess weight at conception is linked to pregnancy complications.
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Genetic testing
Genetic testing can give you vital information if you're planning a family or if you, or your partner, has a genetic disorder.
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Worried about your memory or dementia?
You might be worried that you or a family member has dementia. Learn the early signs of dementia and how to raise concerns with your doctor.
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Tourette syndrome
People with this syndrome make involuntary repetitive sounds and movements. Most don't need treatment, and relaxation exercises may reduce symptoms.
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Tuberous sclerosis
Tuberous sclerosis affects parts of the body, behaviour and thinking. If you notice symptoms you should see a doctor, but there are ways to manage the disease.
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Sickle cell anaemia
Sickle cell anaemia is the most common and serious form of sickle cell disease, in which the body produces too many unstable red blood cells.
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