Search results for Patient support and clinical guidance on rare genetic conditions.

261 - 270 of 1030 results for "Patient support and clinical guidance on rare genetic conditions."

• 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.

• Androgen insensitivity syndrome - Living with

  Find out how, with the appropriate care and support, people with androgen insensitivity syndrome (AIS) can lead full and satisfying lives.

• 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.

• Anxiety in pregnancy

  Find out more anxiety in pregnancy (perinatal anxiety), including signs to look out for, tips to reduce anxiety and information on treatment and support.

• Generalised anxiety disorder (GAD)

  Find out about generalised anxiety disorder (GAD) including the symptoms, causes, how it's diagnosed and the treatment and support available.

• Amyloidosis

  Find out about amyloidosis, including what the symptoms are, when and where to get medical help, the causes and how it's treated.

• Inflammatory bowel disease (IBD)

  Find out about inflammatory bowel disease, including what the symptoms are, how it's treated, what causes it and where you can get support.

• Fibromyalgia

  Fibromyalgia, also called fibromyalgia syndrome (FMS), is a long-term condition that causes pain all over the body.

• What is myelodysplastic syndrome (MDS)?

  Find out about myelodysplastic syndrome (MDS), a rare type of blood cancer.

• Ulcerative colitis

  NHS information about ulcerative colitis, a long-term condition that affects your large bowel (colon).