Search results for Newborn blood spot screening and inherited metabolic conditions.

401 - 410 of 710 results for "Newborn blood spot screening and inherited metabolic conditions."

• Vitamin B12 or folate deficiency anaemia - Symptoms

  Read about the symptoms of vitamin B12 or folate deficiency anaemia, which usually develop gradually, but can worsen if the condition goes untreated.

• Myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS) - Diagnosis

  There's no test for the condition, but there are clear guidelines for diagnosing it.

• Lichen sclerosus

  Read about lichen sclerosus, a skin condition that mainly affects the skin of the genitals.

• Brain abscess

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

• Prader-Willi syndrome

  Find out about Prader-Willi syndrome (PWS), which is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges.

• Craniosynostosis

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

• Continuous glucose monitoring and hybrid closed loop for diabetes

  Find out how a continuous glucose monitor (CGM) or hybrid closed loop system can help you manage your blood glucose (sugar) levels, and how to get one.

• Venous leg ulcer - Causes

  A venous leg ulcer can develop after a minor injury if there is a problem with the circulation of blood in your leg veins.

• Complex regional pain syndrome

  Find out about complex regional pain syndrome (CRPS), a poorly understood condition where a person experiences persistent severe and debilitating pain.

• Corticobasal degeneration

  Read about corticobasal degeneration (CBD), a rare condition where brain cells become damaged over time and certain sections of the brain start to shrink.