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Autor:
Kochlef, Asma, Gargouri, Dalila, Bousnina, Olfa, Romani, Malika, Kilani, Afef, BelHadg, Najet, Kharrat, Jamel, Gorbel, Abdeljabbar, Shili, Sarra, Jemli, Chiraz, Habib Daghfous, Mohamed, Khlifi, Slim, Ben Maamer, Anis, Letaïef, Abdelmajid
Publikováno v:
La Tunisie medicale. 83(8)
Osler Weber Rendu Disease is an hereditary haemorrhagic télangectasia habitually revealed by reccurent bleeding (epistaxis). Hepatic involvement in Osler disease is found in 8 to 31%, manifested by cholestasis. We report an original observation of a