Search results for Rare Genetic Conditions and Inherited Metabolic Disorders.

51 - 60 of 731 results for "Rare Genetic Conditions and Inherited Metabolic Disorders."

• Autosomal recessive polycystic kidney disease - Causes

  Autosomal recessive polycystic kidney disease (ARPKD) is an inherited condition, which means it's passed on to a child from their parents.

• Azathioprine: a medicine to treat autoimmune conditions

  NHS information about the medicine azathioprine including what it's used for, who can take it, how to take it and side effects.

• Haemochromatosis

  Find out about haemochromatosis, an inherited condition where iron levels in the body slowly build up over many years.

• 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.

• Fibromyalgia - Diagnosis

  Diagnosing fibromyalgia can be difficult, as there's no specific test to diagnose the condition.

• Treatment - Binge eating disorder

  Read about treatments for binge eating disorder, including self-help treatments, cognitive behavioural therapy (CBT) and medicines, such as antidepressants.

• Obsessive compulsive disorder (OCD)

  Find out about obsessive compulsive disorder (OCD), what causes it, where to get help, and what the main treatments are.

• Thalassaemia

  Read about thalassaemia, a group of blood disorders that affect a substance called haemoglobin.

• Candesartan: a medicine for blood pressure and heart conditions

  NHS information about the medicine candesartan, including what it's used for, who can take it, how to take it and side effects.

• Developmental co-ordination disorder (dyspraxia) in children

  Read about developmental co-ordination disorder (DCD), also known as dyspraxia, a condition that affects physical co-ordination.