Search Results - "Mahjoub, Bahri"

Kawasaki disease shock syndrome complicated by coronary aneurysms: a case report by Rassas, Ahmed, Guizani, Rihab, Werdani, Amina, Jammeli, Nesrine, Mahjoub, Bahri

“…Kawasaki disease is a generalized systemic vasculitis, which primarily affects medium-sized arteries. Kawasaki disease shock syndrome is a rare but severe…”
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Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation by Sakka, Rania, Mahjoub, Bahri, Kerkeni, Emna, Werdani, Amina, Boussoffara, Raoudha, Ben Cheikh, Hassen, M'rad, Ridha, Sfar, Mohamed Taher

“…Poikiloderma with neutropenia (PN) is a genodermatosis characterized by poikiloderma, permanent neutropenia, recurrent infections, nail abnormalities, and…”
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Orbital complication of acute ethmoiditis: A Tunisian paediatric cross sectional study by Ben Mabrouk, Asma, Wannes, Selmen, Hasnaoui, Mehdi, Werdani, Amina, Ben Hamida, Nouha, Jerbi, Saida, Driss, Nabil, Mahjoub, Bahri

“…The anatomical and developmental particularities of sinus cavities in paediatric population lead acute ethmoiditis to be the earliest form of sinusitis in…”
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Excision of Giant Retroperitoneal Immature Teratoma with post-operative chylous ascites by Mosbahi, Sana, Sallemi, Sahla, Ben Abdejelil, Nouha, Mani, Salma, Ben Youssef, Sabrine, Belhassen, Samia, Achour, Asma, Hidouri, Saida, Wardeni, Amina, Sahnoun, Lassaad, Mekki, Mongi, Belghith, Mohsen, Zakhama, Abdelfatteh, Golli, Mondher, Mahjoub, Bahri, Nouri, Abdellatif

“…Retroperitoneal cystic immature teratoma (RCIT) is a rare disease. Its diagnosis and management are challenging. Although, the prognosis is relatively…”
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Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients by Bouchlaka, Chiraz, Maktouf, Chokri, Mahjoub, Bahri, Ayadi, Abdelkarim, Sfar, M Tahar, Sioud, Mahbouba, Gueddich, Neji, Belhadjali, Zouheir, Rebaï, Ahmed, Abdelhak, Sonia, Dellagi, Koussay

“…Megaloblastic anaemia 1 (MGA1) is a rare autosomal recessive condition characterized by selective intestinal vitamin B12 malabsorption and proteinuria. More…”
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Bilateral orbital myeloid sarcoma as initial manifestation of acute myeloid leukemia by Hmidi, Kamel, Zaouali, Sonia, Messaoud, Riadh, Mahjoub, Bahri, Ammari, Wafa, Bacha, Leila, Laatiri, Adnene, Jenzeri, Salah, Khairallah, Moncef

“…Granulocytic sarcoma is a rare orbital complication of acute leukemia. It concerns primarily children under 10 years of age suffering from primitive acute…”
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Response to growth hormone therapy in ring chromosome 15: Review and evidence from a new case on possible beneficial effect in neurodevelopment by Wannes, Selmen, El Ahmer, Ikram, Rjiba, Khouloud, Jemmali, Nessrine, Abdallah, Hamza Haj, Haj, Rania Bel, Achour, Asma, Bouzidi, Hassan, Saad, Ali, Mougou, Soumaya, Mahjoub, Bahri

“…Type 1 Insulin-like Growth Factor Receptor(IGF1R) plays a fundamental role in normal growth and development. Its disruption is usually characterized by severe…”
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Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment by Khabou, Boudour, Mahjoub, Bahri, Barbu, Véronique, Balhoudi, Nassima, Wardani, Amina, Sfar, Mohamed Taher, Fakhfakh, Faiza

“…Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a chronic autosomal recessive disorder characterized by a wide spectrum of clinical severity…”
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Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia by Najah, Mohamed, Di Leo, Enza, Awatef, Jelassi, Magnolo, Lucia, Imene, Jgurim, Pinotti, Elisa, Bahri, Mahjoub, Barsaoui, Sihem, Brini, Ines, Fekih, Moncef, Slimane, Mohamed Naceur, Tarugi, Patrizia

“…Abetalipoproteinemia (ABL) and Homozygous Familial Hypobetalipoproteinemia (Ho-FHBL) are rare monogenic diseases characterised by very low plasma levels of…”
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Neonatal duodenal obstruction due to a preduodenal portal vein associated with intestinal malrotation: A case report by Ben Hamouda, Hechmi, Hadj Salem, Radhia, Rabeh, Hatem, Ben Amor, Ilhem, Belhassen, Samia, Soua, Hahib, Nouri, Abdellatif, Ben Rhouma, Khaled, Hamza, Hassine, Mahjoub, Bahri, Sfar, Mohamed Tahar

“…Preduodenal portal vein (PDPV) is a rare congenital vascular anomaly in which the portal vein passes unusually anterior to the duodenum rather than…”
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Kawasaki disease shock syndrome complicated by coronary aneurysms: a case report by Rassas, Ahmed, Guizani, Rihab, Werdani, Amina, Jammeli, Nesrine, Mahjoub, Bahri

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Severe community acquired pneumonia due to Staphylococcus aureus in children. About two cases by Bedoui, Abir, Braham, Mounira, Mahjoub, Bahri, Ayadi, Abdelkarim, Ben Homouda, Hechmi, Boussoffara, Raoudha, Ali Lachtar, M, Methlouthi, Jihene, Abid, Faouzi, Sfar, M Taher

“…The staphylococcal pneumonia is the prerogative of the infant but rare cases were observed in the childhood. We report the observation of two children aged…”
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