Search results for Neurofibromatosis

31 - 40 of 223 results for "Neurofibromatosis"

• Charcot-Marie-Tooth disease

  Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that cause nerve damage, leading to muscle weakness and numbness

• Amyloidosis

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

• Morton's neuroma

  Find out about Morton's neuroma, including the symptoms, causes and treatments.

• Peripheral neuropathy - Complications

  Find out about complications of peripheral neuropathy, including foot ulcers, gangrene and cardiovascular autonomic neuropathy (CAN).

• Progressive supranuclear palsy

  Progressive supranuclear palsy (PSP) is a rare neurological condition that can cause problems with balance, movement, vision, speech and swallowing.

• Peripheral neuropathy - Symptoms

  The symptoms of peripheral neuropathy vary according to the type of peripheral neuropathy you have. They may develop quickly or slowly.

• Hereditary haemorrhagic telangiectasia (HHT)

  Read information on hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome), including symptoms, causes and how it's treated.

• Craniosynostosis

  Find out about craniosynostosis, a rare condition where a baby's skull does not grow properly and their head becomes an unusual shape.

• Hypoparathyroidism

  Find out about hypoparathyroidism, including what symptoms it can cause and how it's treated.

• 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.