Search results for Authoritative reference on genetic conditions and pediatric rare diseases.

241 - 250 of 785 results for "Authoritative reference on genetic conditions and pediatric rare diseases."

• Polymyalgia rheumatica

  Find out about polymyalgia rheumatica (PMR), a condition that causes pain, stiffness and inflammation in the muscles around the shoulders, neck and hips.

• Neurofibromatosis type 2

  Find out about neurofibromatosis type 2 (NF2), including what the symptoms are and how it’s treated.

• Ichthyosis

  Find out about ichthyosis, a condition that causes dry scaly skin, including when to get medical help, treatment options and types.

• What complications can affect the placenta?

  These complications are rare.

• Screening for sickle cell and thalassaemia

  Find out about screening for sickle cell and thalassaemia in pregnancy, including how and why it's done, how to get it and when you receive the results.

• Neurofibromatosis type 1 (NF1)

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

• Tourette syndrome

  Find out about Tourette syndrome, a condition that causes tics, including its symptoms, treatment and causes.

• Dupuytren's contracture

  Find out about Dupuytren's contracture (Dupuytren's disease), which affects the hands and fingers and causes 1 or more fingers to bend into the palm of the hand.

• Farting (flatulence)

  Flatulence is passing gas from the digestive system out of the back passage. It's more commonly known as "passing wind", or "farting".

• 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.