Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nadia Mebrouk"'
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
Autor:
Nadia Mebrouk, Boutaina Halimi, Najlae El Attari, Youssra Abdeljalil, Chtouki Loubna, Abdelali Bentahila
Publikováno v:
Asian Journal of Pediatric Research. 12:1-4
We report the case of a 28-month-old boy who displayed symptoms of Henoch-Schonlein purpura (HSP), a type of small-vessel vasculitis that affects multiple systems in childhood and is caused by IgA. The symptoms include dermatological, abdominal, arti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84da783a1c4a54d0309cec7bd8ceda3f
https://doi.org/10.9734/ajpr/2023/v12i3239
https://doi.org/10.9734/ajpr/2023/v12i3239
Publikováno v:
Asian Journal of Pediatric Research. 12:13-22
Kawasaki disease (KD) is a common pediatric vasculitis with a risk of coronary artery aneurysm. In this report, we review some particularities of KD disease, especially coronary involvement, and highlight its aspects during the COVID-19 epidemic whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc90574d78c7a06788ec4c96f53d8905
https://doi.org/10.9734/ajpr/2023/v12i2237
https://doi.org/10.9734/ajpr/2023/v12i2237
Autor:
Nadia Mebrouk, Najlae Attari, Boutaina Halimi, Loubna Chtouki, Najat Lamalmi, Abdelali Bentahila
Publikováno v:
Asian Journal of Pediatric Research. 12:9-12
Sinus histiocytosis, also known as Rosaï Dorfman Syndrome (SRD), is a noncancerous condition that causes the growth of large masses of histiocytes in lymph nodes, primarily in the cervical area. Visceral damage is common, and diagnosis is made throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b8cdec50ce286079f86daf0093d718
https://doi.org/10.9734/ajpr/2023/v12i2236
https://doi.org/10.9734/ajpr/2023/v12i2236
Publikováno v:
Asian Journal of Pediatric Research. :7-10
Macrophage Activation Syndrome (MAS), or Haemophagocytosis Syndrome, is a clinical-biological entity characterized by the proliferation and non-specific activation of macrophages of the reticulo-histiocytic system, with phagocytosis of the blood elem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::425c87b2236ed41898e4973fc4c4b66a
https://doi.org/10.9734/ajpr/2022/v9i330266
https://doi.org/10.9734/ajpr/2022/v9i330266
Autor:
Abdelali Bentahila, Hassan Ait Oamer, Thami Benouachane, Loubna Chtouki, Bouchra Chkirat, Fatima Jabourik, Nadia Mebrouk
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Deficiency rickets due to maternal hypovitaminosis D cause hypocalcaemia in infants, which may be complicated by dilated cardiomyopathy (DCM) with myocardial dysfunction. Calcium is central in myocardial contraction coupling, and hypocalcemia decreas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4be4aef296dd3ea83841a005227beca
https://doi.org/10.9734/ajpr/2022/v9i230260
https://doi.org/10.9734/ajpr/2022/v9i230260
Autor:
Nadia Mebrouk, Yasmine Lachkar, Aziza Bentalha, Latifa Chat, Yamna Kriouile, Asmaa Mdaghri Alaoui
Publikováno v:
International Journal of Innovative Research in Medical Science. 7:244-247
The Covid-19 infection disrupts various organs, including the liver, kidney, and nervous system. Common neurological symptoms of the Covid-19 infection include delirium, confusion, headache, and loss of sense of smell and taste. In rare cases it can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e3428cec305f823209959d7479c48c
https://doi.org/10.23958/ijirms/vol07-i05/1387
https://doi.org/10.23958/ijirms/vol07-i05/1387
Autor:
Nadia. Mebrouk, Sara Benchidmi, Naima El Hafidi, Fadoua Benbrahim, Ghizlane Jaabouti, Najat. Lamalmi, Ali Ayoubi, Soumia Benchekroun, Chafiq Mahraoui
Publikováno v:
International Journal of Innovative Research in Medical Science. 7:240-243
Laryngeal papillomatosis (LP) is a relatively rare benign tumoral proliferation of the larynx, usually seen in children. It is due to infection with Human Papilloma Virus (HPV), and the first symptom is chronic dysphonia. There is currently no consen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83c2ba2abbf04c29d97f561aaa7ab741
https://doi.org/10.23958/ijirms/vol07-i05/1386
https://doi.org/10.23958/ijirms/vol07-i05/1386
Publikováno v:
Asian Journal of Pediatric Research. :9-12
Pycnodysostosis is a rare genetic disease, caused by a mutation of the cathepsin K gene which is involved in bone renewal. It is associated with dwarfism and bone fragility, but the association with a stridor is exceptional. We report the case of a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::954f751e91d889c2e73dcdb2aee5bbf3
https://doi.org/10.9734/ajpr/2022/v8i430249
https://doi.org/10.9734/ajpr/2022/v8i430249
Publikováno v:
Pan African Medical Journal. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8294078cb9e14b5e1155ddbcb48722f4
https://doi.org/10.11604/pamj.2023.44.181.39820
https://doi.org/10.11604/pamj.2023.44.181.39820