Search results for Rare Genetic Syndromes and Family Support Information.

201 - 210 of 1940 results for "Rare Genetic Syndromes and Family Support Information."

• Sharing data from your health records – Information in different languages and formats

  Get information about choosing to share your health record data for planning and research in different formats and languages.

• Epidermolysis bullosa

  Epidermolysis bullosa (EB) is a general term used to describe a group of rare, inherited skin disorders that cause the skin to become very fragile.

• Money, work, benefits and social care - Social care and support guide

  How to pay for care and support, and where you can get help with costs.

• Myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) - Diagnosis

  Find out how myalgic encephalomyelitis (chronic fatigue syndrome or ME/CFS) is diagnosed.

• 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).

• Granulomatosis with polyangiitis (GPA)

  Find out about granulomatosis with polyangiitis (GPA), including what the symptoms are, how it's diagnosed and how it's treated.

• Myositis (polymyositis and dermatomyositis)

  Find out more about myositis, the name for a group of rare conditions that cause muscle weakness.

• Side effects and risks of the combined pill

  Find out about common side effects of the combined pill and some of the rare health risks associated with taking it.

• Autism and adult life

  NHS information about daily life as any autistic adult, what support you might need and where to find it.

• Behçet's disease

  Read about Behçet's disease, a rare and poorly understood condition in which blood vessels and tissues may become inflamed (swollen).