Patient affected by the Osler-Rendu-Weber syndrome

Numéro d’image : 11840137
Patient affected by the Osler-Rendu-Weber syndrome
Close-up of the face of a patient affected by the Osler-Rendu-Weber syndrome also known as hereditary haemorrhagic telangiectasia. This is an inherited condition in which telangiectases,localised collections of distended blood capillaries,develop on the skin and mucous surfaces. They are 2-3mm in diameter,red in colour and become pale when pressed. Other symptoms include nose bleeding and iron-deficiency anaemia resulting from bleeding in the stomach or elsewhere in the gastrointestinal tract. Death very rarely results from uncontrolled gastrointestinal haemorrhage. Treatment is limited to blood or iron replacement
Licence : Droits gérés
Crédit: Science Photo Library / Marazzi, Dr. P.
Taille de l’image : 5066 px × 3543 px
Model Release : Disponible
Property Release : Non requis
Restrictions :
  • Not to be used for advertising or in a defamatory context

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