Search results for NHS UK: Rare Genetic Conditions and Developmental Delays in Children.

281 - 290 of 2007 results for "NHS UK: Rare Genetic Conditions and Developmental Delays in Children."

• Thalassaemia - Symptoms

  Read about the main symptoms of thalassaemia, including anaemia, delayed growth and problems caused by too much iron in the body.

• Brain abscess

  It's a rare and life-threatening condition, usually caused by infection or a severe head injury.

• Psoriasis

  Find out about psoriasis, a long-term skin condition that causes patches of dry, flaky skin that can be itchy and painful.

• Neurofibromatosis type 2

  Find out about neurofibromatosis type 2 (NF2), including what the symptoms are and how it’s treated.

• Report an issue with the NHS website

  Report an issue with the NHS website, like a technical problem or a mistake with the content.

• Neurofibromatosis type 1 (NF1)

  Find out about neurofibromatosis type 1 (NF1), including what the symptoms are and how it’s treated.

• Managing your login settings in the NHS App – NHS App help

  How to change the email address, password and phone number you use to log in to the NHS App.

• Find your NHS number service privacy policy

  Privacy policy for the online Find your NHS number service.

• NHS App privacy and legal information

  Find out more about your privacy when you use the NHS App and other information.

• NHS services