Search results for (2024). Rare Inherited Metabolic Disorders.

111 - 120 of 422 results for "(2024). Rare Inherited Metabolic Disorders."

• Hirschsprung's disease

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

• Paget's disease of the nipple

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

• Chronic obstructive pulmonary disease (COPD) - Treatment

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

• Von Willebrand disease

  Find out about von Willebrand disease, including what the symptoms are, when and where to get medical help, the causes and how it's treated.

• Methylphenidate for children: a medicine used to treat attention deficit hyperactivity disorder (ADHD)

  NHS medicines information on methylphenidate for children – what it's used for, side effects, dosage and who can take it.

• Methylphenidate: a medicine used to treat attention deficit hyperactivity disorder (ADHD)

  NHS medicines information on methylphenidate for adults – what it's used for, side effects, dosage and who can take it.

• What complications can affect the placenta?

  These complications are rare.

• Patau's syndrome

  Find out about Patau's syndrome, also known as trisomy 13, a serious genetic disorder where a baby has an extra copy of chromosome 13.

• Gilbert's syndrome

  Find out about Gilbert's syndrome, a genetic condition where a substance called bilirubin builds up in the blood and causes jaundice.

• What is vulval cancer?

  Find out about vulval cancer, a rare type of cancer sometimes caused by human papillomavirus (HPV).