Search results for NHS UK - Clinical Support and Care Pathways for Rare Genetic Disorders in Children.

391 - 400 of 2121 results for "NHS UK - Clinical Support and Care Pathways for Rare Genetic Disorders in Children."

• Rubella (german measles)

  Find out about rubella (german measles), including what the symptoms are, what to do if you get it and the risks of catching rubella while you’re pregnant.

• NHS App cookies policy

  Find out why we put cookies on your device or browser for the NHS App to work, and why we collect information about how you use the app to help us improve.

• Spina bifida

  Find out about spina bifida, including what causes it, what the symptoms are, how it is treated and what support you might need.

• What is stomach cancer?

  Find out what stomach cancer is, how serious it is, and how common it is in the UK.

• Postnatal depression

  Find out about postnatal depression (PND), including symptoms, treatments, self-care and when to get medical help.

• Myositis (polymyositis and dermatomyositis)

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

• Moving on to adult mental health services

  Find out about moving from children and young people's mental health services to adult services, including the support you'll get during this time

• Antenatal care with twins

  Find out about what tests and scans to expect when you're having twins or more, plus the risks of a twin or triplet pregnancy.

• Neurofibromatosis type 1 (NF1)

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

• Trichotillomania (hair pulling disorder)

  Trichotillomania is when someone cannot resist the urge to pull out their hair.