Complicated meconium ileus in a male neonate with cystic fibrosis: Case report

Autor: Mohamed Sellouti, Aomar Agadr, Rachid Abilkassem

Publikováno v: Radiology Case Reports, Vol 20, Iss 1, Pp 187-190 (2025)

In about 10%-15% of instances, meconium ileus (MI) is the first sign of cystic fibrosis (CF). If a newborn exhibits signs of intestinal obstruction and does not pass meconium within a short period of time after birth, MI is suspected. The cystic fibr

Externí odkaz: https://doaj.org/article/68a3a4b4a8b04ae98c02d72740268155

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A Novel NRAS Variant Near the Splice Junction in Moroccan Childhood Acute Lymphoblastic Leukemia: A Molecular Dynamics Study.

Autor: Skhoun H; Genetics Unit, Military Hospital Mohammed V, Rabat, Morocco.; Laboratory of Human Pathologies Biology and Genomic Center of Human Pathologies, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco., El Fessikh M; Genetics Unit, Military Hospital Mohammed V, Rabat, Morocco.; Laboratory of Human Pathologies Biology and Genomic Center of Human Pathologies, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco., Khattab M; Pediatric Hematology and Oncology Center, Children's Hospital, Rabat, Morocco.; Centre of Childhood Care and Prevention, Cheikh Zaid International University Hospital, Rabat, Morocco., Mchich B; Unité de Biologie Fonctionnelle Et Adaptative, Université Paris Cité, CNRS, INSERM, Paris, France., Agadr A; Department of Pediatrics, Military Hospital Mohammed V, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco., Abilkassem R; Department of Pediatrics, Military Hospital Mohammed V, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco., Dakka N; Laboratory of Human Pathologies Biology and Genomic Center of Human Pathologies, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco., Flatters D; Unité de Biologie Fonctionnelle Et Adaptative, Université Paris Cité, CNRS, INSERM, Paris, France., Camproux AC; Unité de Biologie Fonctionnelle Et Adaptative, Université Paris Cité, CNRS, INSERM, Paris, France., Ouzzif Z; Laboratories Pole, Military Hospital Mohammed V, Rabat, Morocco., El Baghdadi J; Genetics Unit, Military Hospital Mohammed V, Rabat, Morocco. baghdadijamila@yahoo.fr.; Laboratories Pole, Military Hospital Mohammed V, Rabat, Morocco. baghdadijamila@yahoo.fr.

Publikováno v: Biochemical genetics [Biochem Genet] 2024 Nov 08. Date of Electronic Publication: 2024 Nov 08.

Vitamin B12 deficiency: case report and review of literature

Autor: Brahim El Hasbaoui, Nadia Mebrouk, Salahiddine Saghir, Abdelhkim El Yajouri, Rachid Abilkassem, Aomar Agadr

Publikováno v: The Pan African Medical Journal, Vol 38, Iss 237 (2021)

Vitamin B12 deficiency in early childhood is an important cause of neurodevelopmental delay and regression. Most of these cases occur in exclusively breast-fed infants of deficient mothers. Symptoms and signs of vitamin B12 deficiency appear between

Externí odkaz: https://doaj.org/article/2ea963f42f5f4bae86405b2679878377

Triple X Syndrome with Congenital Anomalies: A Rare Case Report

Autor: A. Agadr, R. Abilkassim, M. Sellouti, A. Ayad, S. Saghir, E. Bahous

Publikováno v: Asian Journal of Pediatric Research. :1-5

Triple X syndrome is a relatively common chromosomal abnormality affecting 0.1% of live-born girls. Most of these girls have a normal phenotype and only a few cases have birth defects. The diagnosis of triple X syndrome may never be made because the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6fc1a19c99cc29a0a15940db2b9343b7
https://doi.org/10.9734/ajpr/2023/v11i2214