Search results for Rare Genetic Conditions and Inherited Metabolic Disorders.

11 - 20 of 731 results for "Rare Genetic Conditions and Inherited Metabolic Disorders."

• Polyendocrine metabolic ovarian syndrome (PMOS)

  Find out about polyendocrine metabolic ovarian syndrome (PMOS), previously called polycystic ovary syndrome, including what the symptoms are, how it's diagnosed and what the treatments are.

• Auditory processing disorder (APD)

  Find out about auditory processing disorder, a condition where you have difficulty understanding sounds including spoken words.

• Genetic tests to check your cancer risk

  Find out about genetic tests for cancer risk, including why they are done, how to get them, what happens, and when you'll get your results.

• Conditions A to Z: common topics

  Find health conditions from our A to Z list of common topics, including the symptoms and how they're treated.

• Content not licensed for re-use - Terms and conditions

  Content not licensed under the standard NHS website terms and conditions.

• Epidermolysis bullosa

  Epidermolysis bullosa (EB) is a general term used to describe a group of rare, inherited skin disorders that cause the skin to become very fragile.

• 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.

• Hoarding disorder

  Find out about hoarding disorder, including the symptoms, causes, how it’s diagnosed and treated and where to get support.

• Generalised anxiety disorder (GAD)

  Find out about generalised anxiety disorder (GAD) including the symptoms, causes, how it's diagnosed and the treatment and support available.

• Viewing health conditions – NHS App help

  Find out how to view information about your health conditions in the NHS App.