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

211 - 220 of 2007 results for "NHS UK: Rare Genetic Conditions and Developmental Delays in Children."

• Patau's syndrome

  Find out about Patau's syndrome, also known as trisomy 13, a serious genetic disorder where a baby has an extra copy of chromosome 13.

• Ankylosing spondylitis - Symptoms

  The symptoms of ankylosing spondylitis (AS) can vary from person to person, but usually develop slowly over several months or years.

• NHS App

  Use the NHS App to view your health information and manage your healthcare online using a phone, tablet or computer.

• Help and support for a malignant brain tumour (brain cancer)

  Find out where to get help and support for a malignant brain tumour (brain cancer) from your specialist team and charities like Macmillan or Cancer Research UK.

• NHS gender dysphoria clinics

  You and your GP may agree that you should see specialists at a gender dysphoria clinic so you can consider your treatment options. Here's how to find one.

• Malnutrition – Symptoms

  Find out about the symptoms of malnutrition in adults and children.

• Appointments – NHS App help

  How to book and manage GP and hospital appointments, or contact your GP surgery using the NHS App.

• Who can use the NHS App – NHS App help

  You can use the NHS App if you’re aged 13 or over and registered at an NHS GP surgery in England or the Isle of Man.

• Logging in to the NHS App – NHS App help

  Read about how to log in to the NHS App and how to get help with problems.

• Ménière's disease

  Find out more aboaut Ménière's disease, a rare condition that affects the inner ear.