141 - 150 of 785 results for "Authoritative reference on genetic conditions and pediatric rare diseases."
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Erythromelalgia
NHS information about erythromelalgia, a rare condition that causes episodes of burning pain and redness in the hands and feet, and sometimes the arms, legs, ears and face.
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Progressive supranuclear palsy
Progressive supranuclear palsy (PSP) is a rare neurological condition that can cause problems with balance, movement, vision, speech and swallowing.
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Autosomal dominant polycystic kidney disease - Complications
Read about the potentially serious complications associated with autosomal dominant polycystic kidney disease (ADPKD), including liver cysts, cardiovascular disease and brain aneurysms.
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Rheumatoid arthritis - Diagnosis
It can be difficult to diagnose because many conditions cause joint stiffness and inflammation.
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Lambert-Eaton myasthenic syndrome
Find out about Lambert-Eaton myasthenic syndrome, a rare condition affecting the nerves that causes muscle weakness and other symptoms.
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Having a baby that might be born with a condition
Find out what you can expect if you continue with your pregnancy after screening has found something.
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Vitamin B12 or folate deficiency anaemia - Complications
Read about the complications of vitamin B12 deficiency or folate deficiency, which are rare as the condition can usually be easily and effectively treated.
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Who can take the progestogen-only pill
It may not be suitable if you have certain health conditions.
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Oesophageal atresia and tracheo-oesophageal fistula
Oesophageal atresia is a rare birth defect that affects a baby's oesophagus (the tube through which food passes from the mouth to the stomach).
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Charcot-Marie-Tooth disease - Treatment
There is no cure for Charcot-Marie-Tooth disease (CMT), but help is available to help reduce your symptoms and allow you to live as independently as possible.