Search results for Chromosome 22 Deletion and Rare Syndromes. UK Medical Guidelines.

141 - 150 of 846 results for "Chromosome 22 Deletion and Rare Syndromes. UK Medical Guidelines."

• Herpes simplex eye infections

  Find out about herpes simplex eye infections, including what the symptoms are, when and where to get medical help and how they're treated.

• Whooping cough

  Find out about whooping cough, including the symptoms, who's at risk, when to get medical advice, how it's treated and the whooping cough vaccine.

• Oesophageal atresia and tracheo-oesophageal fistula

  Oesophageal atresia is a rare birth defect that affects a baby's oesophagus (the tube through which food passes from the mouth to the stomach).

• Erythromelalgia

  NHS information about erythromelalgia, a rare condition that causes episodes of burning pain and redness in the hands and feet, and sometimes the arms, legs, ears and face.

• Peripheral neuropathy - Causes

  In the UK, the most common cause of peripheral neuropathy is diabetes.

• NHS App accessibility statement - Version 10.1, 22 December 2025

  Find out more about how accessible the NHS App is, and how make sure as many people as possible can use it.

• Roseola

  Find out about the childhood infection roseola, including what the symptoms are, how to treat it and when to get medical advice.

• 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.

• Symptoms of vascular dementia

  Read about the main symptoms of vascular dementia and find out when to get medical advice.

• Thalassaemia

  Read about thalassaemia, a group of blood disorders that affect a substance called haemoglobin. Find out about the symptoms, causes and treatments.