Search Results - "Douira, W"

Cryptorchidism in children: Predictive factors of orchidopexy failure and postoperative testicular atrophy by Boulma, R, Ben Chouchen, I, Nouira, F, Ben Ahmed, Y, Boukesra, T, Chibani, I, Lahmar, L, Charieg, A, Mamlouk, A, Douira, W, Jlidi, S

“…Outcomes of orchidopexy for undescended testes may be disappointing. The aim of our study was to identify predictive factors of testicular atrophy and…”
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Partial third nerve palsy revealing cerebral cavernomatosis by Malek, I., Sayadi, J., Mekni, M., Lahmer, A., Henchiri, M., Douira, W., Nacef, L.

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Deep venous thrombosis associated with acute hematogenous osteomyelitis in children by Bouchoucha, S, Benghachame, F, Trifa, M, Saied, W, Douira, W, Nessib, M.N, Ghachem, M.B

“…Summary Introduction Deep venous thrombosis (DVT) is rare in children. It may complicate acute hematogenous osteomyelitis (AHO). Objective The present study…”
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Vertebral collapse revealing primary hyperparathyroidism in a 14-year-old girl by Ben Hassine, L, Lahmar, L, Bouaziz, M, Ammar, I, Louati, H, Douira, W, Nessib, M N, Bellagha, I

“…Primary hyperparathyroidism, widely prevalent in women after menopause, remains rare in children and adolescents. Sporadic forms are the most frequent…”
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Wolman disease by Ben Hassine, L, Lahmar, L, Louati, H, Douira, W, Bellagha, I

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A rare cause of adrenal calcifications by Ben Hassine, L, Lahmar, L, Louati, H, Douira, W, Bellagha, I

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Spontaneous orbital hematoma: two case reports by Louati, H, Hedhli, M, Chebbi, A, Ben Hassine, L, Douira, W, Lahmar, L, Ayed, S, Bellagha, I

“…Although rare, spontaneous intra-orbital hematoma can quickly jeopardize vision. It usually presents with painful proptosis. It can result from multiple…”
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Dysplasia epiphysealis hemimelica: A report of four cases by Douira-Khomsi, W., MD, Louati, H., MD, Mormech, Y., MD, Saied, W., MD, Bouchoucha, S., MD, Smida, M., MD, Ghachem, M. Ben, MD, Hammou, A., MD, Bellagha, I., MD

“…Abstract Dysplasia epiphysealis hemimelica (DEH), also known as Trevor's disease, is a rare congenital skeletal developmental disorder in childhood. It is…”
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Congenital generalized lipodystrophy: a case report with neurological involvement by Ben Turkia, H, Tebib, N, Azzouz, H, Abdelmoula, M Slim, Ben Chehida, A, Hubert, P, Douira, W, Ben Dridi, M F

“…Congenital generalized lipodystrophy (CGL) is a rare disorder characterized by near complete absence of adipose tissue from birth. At least 2 genes located in…”
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Hématome orbitaire spontané : à propos de deux cas by Louati, H., Hedhli, M., Chebbi, A., Ben Hassine, L., Douira, W., Lahmar, L., Ayed, S., Bellagha, I.

“…Bien que rare, l’hématome intra-orbitaire spontané peut mettre en péril rapidement le pronostic visuel. Il se manifeste le plus souvent par une exophtalmie…”
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Imaging features of spinal epidural cavernous malformations by Nagi, S., Megdiche, H., Bouzaïdi, K., Haouet, S., Khouja, N., Douira, W., Sebaï, R., Chaabene, S., Zitouna, M., Touibi, S.

“…Cavernous angioma or cavernoma is a vascular malformation that may affect any area in the neuraxis. Epidural location is very rare and therefore seldom…”
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Une cause inhabituelle de convulsions révélée à l’âge de 4 ans by Louati, H., Miladi, S., Ben Hassine, L., Douira, W., Lahmar, L., Karkani, A., Bellagha, I.

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An uncommon cause of convulsions revealed in a 4-year-old girl by Louati, H, Miladi, S, Ben Hassine, L, Douira, W, Lahmar, L, Karkani, A, Bellagha, I

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Les aspects pathologiques du diverticule de Meckel chez l’enfant by Khemekhem, R., Ben Ahmed, Y., Rahay, H., Soufiane, G., Said, J., Douira, W., Ibtisem, B., Béji, C.

“…Quoi que rare, le diverticule de Meckel (DM) reste l’anomalie congénitale la plus fréquente de l’intestin grêle. Le plus souvent latent, mais peut être la…”
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Intrapancreatic duodenal duplication causing acute abdominal symptoms by Douira, W, Hedhli, M, Louati, H, Sahli, S, Ben Hassine, L, Lahmar, L, Bellagha, I, Hamzaoui, M

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Duplication duodénale intrapancréatique : une cause rare de douleurs abdominales aiguës by Douira, W., Hedhli, M., Louati, H., Sahli, S., Ben Hassine, L., Lahmar, L., Bellagha, I., Hamzaoui, M.

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Burkitt lymphoma in a child with Bloom syndrome by Fedhila-Ben Ayed, F., Douira-Khomsi, W., Rhayem, S., Jelassi, M., Zribi, H., Chaabouni, M., Khemiri, M., Bellagha, I., Barsaoui, S.

“…Bloom syndrome is a rare disease characterized by chromosomal instability and increased risk of developing lymphoma. We report on a case of Bloom syndrome in a…”
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Les kystes et tumeurs de l’ovaire chez l’enfant tunisien. Aspects diagnostiques et prise en charge thérapeutique by Khemakhem, R., Ben Ahmed, Y., Ben Ftina, W., Nouira, F., Charieg, A., Ghorbel, S., Jlidi, S., Chennoufi, F., Barsaoui, S., Douira, W., Bellagha, I., Chaouachi, B.

“…Les masses ovariennes sont rares à l’âge pédiatrique et sont représentées essentiellement par les kystes fonctionnels et les tumeurs bénignes dont le plus…”
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Syndrome de la pince mésentérique chez l’enfant : à propos d’un cas by Khemakhem, R., Ben Dhaou, M., N.Sarray, ould Med Sghaier, Y., Charieg, A., Douira, W., Nouira, F., Ghorbel, S., Jlidi, S., Bellagha, I., Chaouachi, B.

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Lipodystrophie congénitale généralisée de type 1 avec atteinte neurologique by Ben Turkia, H., Tebib, N., Azzouz, H., Slim Abdelmoula, M., Ben Chehida, A., Hubert, P., Douira, W., Ben Dridi, M.F.

“…La lipodystrophie congénitale généralisée est un syndrome rare caractérisé par l’absence complète de tissu adipeux depuis la naissance. Au moins 2 gènes…”
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