51 - 60 of 519 results for "Genetic and rare disease guidance."
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Parkinson's disease - Symptoms
The symptoms of Parkinson's disease usually develop gradually and are mild at first.
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Prader-Willi syndrome - Diagnosis
It can usually be diagnosed using a series of genetic tests.
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Chronic kidney disease
Find out what chronic kidney disease (CKD) is, including what the symptoms are, how it's diagnosed and how it can be treated.
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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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Chronic kidney disease - Diagnosis
Find out how chronic kidney disease (CKD) is diagnosed, who should get tested and what the stages of CKD mean.
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Chronic kidney disease - Symptoms
Find out about the main symptoms of chronic kidney disease (CKD) and when to get medical advice.
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Rett syndrome
Read about Rett syndrome, a rare genetic disorder that affects brain development and causes severe physical and mental disability from early childhood.
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Paget's disease of bone - Diagnosis
Find about the main tests used to diagnose Paget's disease of bone, including blood tests, X-rays and scans.
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Parkinson's disease - Treatment
There's currently no cure for Parkinson's disease, but treatments are available to help relieve the symptoms and maintain your quality of life.
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Autosomal dominant polycystic kidney disease
Find out about autosomal dominant polycystic kidney disease (ADPKD), an inherited condition that causes small fluid-filled sacs called cysts to develop in the kidneys.