121 - 130 of 1006 results for "Rare Genetic Conditions and Support."
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Further help and support for IBS (irritable bowel syndrome)
Find out where to get help and support for IBS (irritable bowel syndrome).
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Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that cause nerve damage, leading to muscle weakness and numbness
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Progressive supranuclear palsy - Diagnosis
It can be difficult to diagnose progressive supranuclear palsy (PSP), as there’s no single test for it, and it can have similar symptoms to other conditions.
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Bisoprolol: a beta blocker medicine for blood pressure and heart conditions
NHS information about the medicine bisoprolol, including what it's used for, who can take it, how to take it and side effects.
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Rheumatoid arthritis - Complications
Having rheumatoid arthritis can put you at a higher risk of developing other conditions.
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Aspergillosis
Find out more about aspergillosis, the name of a group of conditions caused by a mould called aspergillus.
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Further help and support with breast screening
Get more information and support about breast screening, including information in other formats.
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Prader-Willi syndrome - Causes
It's a genetic condition that's the result of a change on chromosome number 15.
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Is my child too ill for school?
Find out when it's best to keep your sick child at home and when it's OK to send them to school or nursery.
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Mastocytosis
Read about mastocytosis, a rare condition caused by an excess number of mast cells gathering in the body's tissues.