11 - 20 of 809 results for "Rare Genetic Syndromes and Support."
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Patau's syndrome
Find out about Patau's syndrome, also known as trisomy 13, a serious genetic disorder where a baby has an extra copy of chromosome 13.
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Prader-Willi syndrome - Diagnosis
Find out how Prader-Willi (PWS) syndrome is diagnosed.
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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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Medical support for people with Down's syndrome
If you have Down's syndrome, you should see a GP once a year for a check-up.
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Sjögren's syndrome
Find out about Sjögren's syndrome, including the symptoms, things you can do to ease them, causes, how it's diagnosed and the treatment and support available.
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Edwards' syndrome
Find out about Edwards’ syndrome (trisomy 18) including the symptoms, types, how it's diagnosed and what causes it.
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Gilbert's syndrome
Find out about Gilbert's syndrome, a genetic condition where a substance called bilirubin builds up in the blood and causes jaundice.
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Cyclical vomiting syndrome
Find out about cyclical vomiting syndrome including the symptoms, causes, how it's diagnosed and the treatment and support available.
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Brugada syndrome
Find out about Brugada syndrome, including what the symptoms are, when and where to get medical help, the causes and how it's treated.
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Causes of myelodysplastic syndrome (MDS)
Find out about the causes of myelodysplastic syndrome (MDS), and who is most at risk of getting it.