261 - 270 of 2052 results for "Rare Genetic Conditions and Heart Health. Available from: NHS Health A-Z."
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Prader-Willi syndrome
Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.
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Thalassaemia - Thalassaemia carriers
Read about how to find out if you're a carrier of thalassaemia and what it means for your health and any children you have.
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Coronary artery bypass graft
Find out what a coronary artery bypass graft (CABG, also called heart bypass surgery) involves, when it might be recommended, and how it can help with coronary heart disease.
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Benefits of exercise
Find out how regular exercise can help you lose weight, boost your mood and reduce your risk of developing long-term conditions.
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Services and support for parents
Advice and information about what's available to new parents through the NHS, local authority services, helplines, charities and local parent groups.
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Digoxin: medicine for heart rhythm problems and heart failure
NHS information about digoxin, including what it's used for, who can use it, how to use it and side effects.
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Fibromyalgia - Diagnosis
Diagnosing fibromyalgia can be difficult, as there's no specific test to diagnose the condition.
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Turner syndrome
Find out about Turner syndrome including the symptoms, how it’s diagnosed and the treatment and support that is available.
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Congenital heart disease in pregnancy
Find out about the risks of congenital heart disease in pregnancy, and where to get support.
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Statins
Find out more about statins, including the conditions they can help treat, common side effects and who can take them.