Search Results - "Abidi, Kamel"

Infantile Parotid Hemangioma With Diagnostic Dilemma: A Case Report by Abidi, Kamel T, Kamal, Naglaa M, Althobaiti, Khaled A, Althobaiti, Sami D, Halabi, Yasser A, Alalyani, Saad A

“…Introduction: Salivary gland tumors are uncommon in children; hemangiomas are one of them. We report a case of infantile hemangioma of the parotid gland which…”
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Diffuse Mesangial Sclerosis in a Child With Dyskeratosis Congenita Leading to End-stage Renal Disease by Kamel, Abidi, Sayari, Taha, Jellouli, Manel, Hammi, Yousra, Louzir, Rim Ghoucha, Gargah, Tahar

“…Dyskeratosis congenita (DC) is a very rare inherited disorder. It is caused by dysfunction of telomere maintenance. It involves RNA telomerase components…”
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Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation by Abidi, Kamel T., Kamal, Naglaa M., Bakkar A., Ayman A., Alotaibi, Maram, Asseri, Haifa, Bokari, Kawthar A.

“…Backgroundd Sjogren–Larsson syndrome (SLS) is a rare autosomal recessive disorder, characterized by a triad of spastic tetraplegia or diplegia, congenital…”
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Primary hyperoxaluria in infants by Jellouli, Manel, Firjani, Maryam, Abidi, Kamil, Zarruq, Shukri, Naija, Ouns, Abd al-Mawla, J., Gargah, Tahar

“…The infantile form of primary hyperoxaluria type-1 (PH-1) is characterized by a rapid progression to the end-stage renal disease (ESRD) due to both increased…”
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Infantile cystinosis : from dialysis to renal transplantation by Abd al-Mawla, Juwaydah, Zarruq, Shukri, Abidi, Kamil, Jellouli, Manel, Gargah, Tahar, Farjani, Maryam

“…Cystinosis is an autosomal recessive, lysosomal storage disease characterised by the accumulation of the amino acid cystine in different organs and tissues. It…”
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Tuberculosis following kidney transplantation: report of paediatric case by Abidi, Kamel, Jellouli, Manel, Hammi, Yousra, Gargah, Tahar

“…Recipients of solid organ transplantation are, because of immunosuppressive therapy, at high risk to develop opportunistic infections including tuberculosis…”
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Williams-Beuren syndrome associated with single kidney and nephrocalcinosis: a case report by Abidi, Kamel, Jellouli, Manel, Ben Rabeh, Rania, Hammi, Yousra, Gargah, Tahar

“…Williams-Beuren syndrome is a rare neurodevelopmental disorder, characterized by congenital heart defects, abnormal facial features, mental retardation with…”
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Persistent Hypertransaminasemia Uncovered Occult Limb-Girdle-Muscle Dystrophy-Type-2C in a Saudi Child by Kamal, Naglaa M, Alghamdi, Hamed A, Halabi, Abdulrahman, Alharbi, Abdullah O, Rafque, Muhammad, Abidi, Kamel, El-Shabrawi, Mortada H.H, Eskander, Ayman E, Mansour, Hala, Sherief, Laila M

“…An asymptomatic 4.5 years-old Saudi girl was referred to the pediatric hepatology service with presumed liver disease because of the persistently elevated…”
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Syndrome de Protée: à propos d'une observation pédiatrique by Kamel Abidi, Manel Jellouli, Abir Boussetta, Yousra Hammi, Tahar Gargah

“…Le syndrome de Protéeest une maladie très rare, se traduisant par une croissance excessive pouvant toucher différents organes et tissus de l'organisme. Ses…”
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Caractéristiques bactériologiques des infections de liquide de dialyse péritonéale by Jellouli, Manel, Ferjani, Meriem, Abidi, Kamel, Hammi, Yosra, Abdallah, Taieb Ben, Gargah, Tahar

“…La péritonite infectieuse (PI) est la principale complication de la dialyse péritonéale (DP). L'objectif de notre travail était de déterminer l’écologie…”
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Particularité de la cystinose infantile chez l'enfant tunisien by Jellouli, Manel, Turkia, Hadhami Ben, Abidi, Kamel, Hammi, Yosra, Gargah, Tahar

“…La cystinose est une maladie rare qui résulte d'un défaut d'expression de la cystinosine transporteur de la cystine du lysosome. La forme infantile est la plus…”
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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients by M'dimegh, Saoussen, Aquaviva‐bourdain, Cécile, Omezzine, Asma, Souche, Geneviéve, M'barek, Ibtihel, Abidi, Kamel, Gargah, Tahar, Abroug, Saoussen, Bouslama, Ali

“…Background Primary hyperoxaluria type 3 (PH3) is due to mutations in the recently identified 4‐hydroxy‐2‐oxoglutarate aldolase (HOGA1) gene. PH3 might be the…”
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Outcome of rapidly progressive glomerulonephritis post-streptococcal disease in children by Jellouli, Manel, Maghraoui, Sondos, Abidi, Kamel, Hammi, Yosra, Goucha, Rim, Naija, Ouns, Zarrouk, Chokri, Gargah, Tahar

“…Rapidly progressive glomerulonephritis is a rare form of postinfectious glomerulonephritis. The aim of this study was to describe the outcome of our patients…”
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Persistance de la veine cave supérieure gauche: à propos d’un cas by Abidi, Kamel, Jellouli, Manel, Hammi, Yousra, Gargah, Tahar

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Focal segmental glomerulosclerosis in children by Jellouli, Manel, Abidi, Kamel, Askri, Mouna, Ferjani, Meriem, Naija, Ouns, Hammi, Yousra, Goucha, Rym, Gargah, Tahar

“…Background Focal segmental glomerulosclerosis (FSGS) represents 20% of nephrotic syndrome in children. The clinical course and prognosis is heterogeneous in…”
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A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype–phenotype correlation by M’DIMEGH, SAOUSSEN, AQUAVIVA-BOURDAIN, CÉCILE, OMEZZINE, ASMA, M’BAREK, IBTIHEL, SOUCHE, GENEVIÉVE, ZELLAMA, DORSAF, ABIDI, KAMEL, ACHOUR, ABDELATTIF, GARGAH, TAHAR, ABROUG, SAOUSSEN, BOUSLAMA, ALI

“…Primary hyperoxaluria type I (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal…”
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Etiologies of end-stage renal disease of children in Tunisia by Jellouli, Manel, Boussetta, Abir, Abidi, Kamel, Maalej, Bayen, Naija, Ouns, Hammi, Yousra, Zarrouk, Chokri, Mahfoudh, Abdelmajid, Gargah, Tahar

“…The end-stage renal disease (ESRD) in children has special features in terms of etiologies, therapeutic modalities and access to renal transplantation. In…”
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Mycophenolate mofetil in treatment of childhood steroid-dependent nephrotic syndrome by Jellouli, Manel, Fitouhi, Sonia, Abidi, Kamel, Hammi, Yousra, Naija, Ouns, Zarrouk, Chokri, Gargah, Tahar

“…To establish the efficacy of mycophenolate mofetil (MMF) in steroid dependent nephrotic syndrome and to determine the predictive factors for a good response…”
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Peritoneal dialysis: Experience of the department of pediatrics of the hospital Charles Nicolle of Tunis by Jellouli, Manel, Ferjani, Meriem, Oueslati, Amal, Abidi, Kamel, Naija, Ouns, Hammi, Yousra, Ben Abdallah, Taieb, Gargah, Tahar

“…Introduction Peritoneal dialysis (PD) is still the most common modality used in treatment for children with End Stage Renal Disease (ESRD). The objective of…”
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Contribution of ultrasound scans in the first episode of urinary tract infection in children by Jellouli, Manel, Ben Mansour, Asma, Abidi, Kamel, Ferjani, Meriem, Naija, Ouns, Hammi, Yousra, Zarrouk, Chokri, Gargah, Tahar

“…Background - Vesicoureteral reflux (VUR) is a common pediatric urologic disorder. After the first urinary tract infection (UTI), imaging studies are…”
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