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[Gillespie syndrome: 2 familial cases].
Arch Pediatr
October 2006
Service de Pédiatrie, Hôpital Farhat-Hached, 4000 Sousse, Tunisie.
We report 2 familial cases of Gillespie syndrome in an 8-year-old girl and her brother 16 months old. They had both congenital aniridia, cerebellar ataxia and mental retardation. In the girl, pupillar dilation in the 2 eyes and delay in different milestones development were elicited at 2 years.
View Article and Find Full Text PDF[Hemolytic-uremic syndrome secondary to scorpion envenomation (apropos of 2 cases)].
Nephrologie
June 2004
Service de réanimation médicale CHU Habib Bourguiba, Sfax.
HUS was recently described following scorpion sting. We report 2 cases of HUS in the intensive care unit of a university hospital. Two children aged respectively 10 months and 1 year were admitted in the ICU after severe scorpion envenomation (with coma and pulmonary oedema) having required dobutamine and mechanical ventilation.
View Article and Find Full Text PDF[Fernand Widal syndrome: apropos of 2 cases].
Dakar Med
June 2002
Service de Pneumophtisiologie C.H.U. de FANN BP: 5035 Dakar/Fann.
The Fernand Widal syndrome combines a nasal polyposis, an asthma and aspirin sensitivity. It remains a nosological entity often unrecognized because of the trivialization of aspirin in-take on the one hand the other its etiopathogenesis which has not yet been clarified because of the inhibition of the cyclo-oxygenase. In actual fact the aspirin molecule has yet to reveal all its secrets (advantages and disadvantages).
View Article and Find Full Text PDF[Formation of a descemetic bleb after deep sclerectomy and visco-canalostomy: apropos of 2 cases].
Klin Monbl Augenheilkd
May 2001
Hôpital de la Ville, Chasseral 20, CH-2300 La Chaux-de-Fonds.
Background: Deep sclerectomy with visco-canalostomy is a new non perforating method for the surgical treatment of glaucoma.
Patients And Methods: We report 2 patients who developed a descemetic bleb after this surgical procedure.
Results: The cornea remained clear for more than ten months, as long as the bleb was not ruptured.
[Duodenal somatostatinomas associated with von Recklinghausen's neurofibromatosis. Apropos of 2 cases].
Ann Pathol
December 2000
Service d'Anatomie et de Cytologie Pathologiques. CHR d'Orléans, 14, avenue de l'Hôpital, BP 6709, 45067 Orléans.
Somatostatinomas are rare neuroendocrine tumors; they are essentially located in the pancreas and in the duodenum. The association with a neurofibromatosis type I is especially observed when the tumor is located in the ampulla of Vater. These tumors are not associated with a "somatostatin syndrome", but often present with gastrointestinal bleeding, abdominal pain and obstructive jaundice.
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