Search results for Rare Genetic Syndromes and Family Support Information.

311 - 320 of 1940 results for "Rare Genetic Syndromes and Family Support Information."

• Developmental dysplasia of the hip

  Find out about developmental dysplasia of the hip (DDH), including how it affects a baby or infant, how it's diagnosed and how it can be treated.

• Progressive supranuclear palsy

  Progressive supranuclear palsy (PSP) is a rare neurological condition that can cause problems with balance, movement, vision, speech and swallowing.

• Side effects and risks of the contraceptive patch

  Find out about common side effects of the contraceptive patch and some of the rare health risks associated with using it.

• Phaeochromocytoma

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

• Malnutrition – Treatment

  Find out about treatments for malnutrition, including dietary changes and supplements, feeding tubes, and care and support services.

• 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.

• 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.

• 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.