Search results for Rare Genetic Syndromes and Support.

251 - 260 of 808 results for "Rare Genetic Syndromes and Support."

• Phaeochromocytoma

  Read about phaeochromocytoma, a rare tumour of the adrenal glands, which is often treated using surgery.

• 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.

• Neurofibromatosis type 1 (NF1)

  Find out about neurofibromatosis type 1 (NF1), including what the symptoms are and how it’s treated.

• Autosomal recessive polycystic kidney disease

  Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited childhood condition where the development of the kidneys and liver is abnormal.

• Chronic obstructive pulmonary disease (COPD) - Treatment

  Find out about the main treatments for COPD, including inhalers, medicine and surgery in rare cases.

• Ménière's disease

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

• Hirschsprung's disease

  Hirschsprung's disease is a rare bowel condition that is mainly diagnosed in babies and young children.

• Side effects and risks of the diaphragm or cap

  Find out about the side effects of the diaphragm or cap and the possible health risks linked to using it.

• Paget's disease of the nipple

  It's a rare condition where eczema-like changes occur in the skin of the nipple and areola.

• What complications can affect the placenta?

  These complications are rare.