171 - 180 of 785 results for "Authoritative reference on genetic conditions and pediatric rare diseases."
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Autosomal recessive polycystic kidney disease - Symptoms
Read about the symptoms of autosomal recessive polycystic kidney disease (ARPKD) that can occur before or soon after birth and during infancy and childhood.
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Autosomal recessive polycystic kidney disease - Diagnosis
A diagnosis of autosomal recessive polycystic kidney disease (ARPKD) is usually based on a child's symptoms and the results of an ultrasound scan.
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Vertigo
Vertigo is a symptom, rather than a condition in itself.
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Emollients
They're often used to treat skin conditions like eczema.
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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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Fibromyalgia - Causes
It's not clear why some people develop fibromyalgia. The exact cause is unknown, but it's likely that a number of factors are involved.
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Betahistine: a medicine used to treat Ménière's disease
NHS information about the medicine betahistine, including what it's used for, who can take it, how to take it and side effects.
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Cholesteatoma
Find out about cholesteatoma, a rare ear condition that causes hearing and balance problems, including the symptoms, when to get medical help and treatments.
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Memantine: a medicine used to treat Alzheimer's disease
NHS medicines information about memantine, including what it's used for, who can take it, how to take it and side effects.
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Hereditary spastic paraplegia
Find out about hereditary spastic paraplegia (HSP), a rare group of inherited disorders that often cause weakness and stiffness in the leg muscles, which gradually gets worse over time.