Zobrazeno 1 - 10
of 287
pro vyhledávání: '"Agadr A"'
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
Publikováno v:
The Pan African Medical Journal, Vol 23, Iss 242 (2016)
Nous apportons une observation d'un cas de la maladie de Wilson, révélé par un syndrome parkinsonien. Le diagnostic a reposé sur les troubles neuropsychiques, la présence de l'anneau cornéen de Kayser-Fleischer, et les troubles du métabolisme
Externí odkaz:
https://doaj.org/article/398c56ff2fe5416182384a2176f444a2
Autor:
Skhoun, Hanaa, El Fessikh, Meriem, El Alaoui Al Abdallaoui, Mohamed, Khattab, Mohammed, Belkhayat, Aziza, Chebihi, Zahra Takki, Hassani, Amale, Abilkassem, Rachid, Agadr, Aomar, Dakka, Nadia, El Baghdadi, Jamila
Publikováno v:
In Archives de pédiatrie May 2024 31(4):238-244
Akademický článek
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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
Publikováno v:
PAMJ Clinical Medicine, Vol 4, Iss 40 (2020)
Une jeune fille de 15 ans, se présente aux urgences pédiatriques pour des douleurs abdominales. Il s´avère à l´interrogatoire que la symptomatologie remonte à 1 mois. La patiente a bénéficié d´une appendicectomie 15 jours auparavant n´aya
Externí odkaz:
https://doaj.org/article/26bca0d50ad940fdabe62e74d8ad5fb6
Publikováno v:
Asian Journal of Pediatric Research. :14-27
Introduction: Pediatric Multisystem Inflammatory Syndrome linked to temporal with SARS-Cov2 is a new hyper inflammatory disorder that affects children with Covid-19 infection. It usually occurs 2 to 6 weeks following illness or exposure. Materials an
Publikováno v:
Scholars Journal of Medical Case Reports. 10:1118-1121
Pompe disease, is a rare severe, autosomal, recessive, and progressive genetic disorder caused by deficiency in alpha-glucosidase. The classic infantile-onset is the most broadly known form of Pompe disease, which presents with severe heart involveme
Publikováno v:
Asian Journal of Pediatric Research. :32-36
Hydrops fetalis is defined by the accumulation of fluids in the serous membranes (pleurisy, ascites, pericarditis...), it is a rare condition; its etiologies are divided into immunological and non-immunological. Supraventricular tachycardia remains a
Autor:
Aomar Agadr, Amal Hassani, Rachid Abilkassem, Abdelhakim Ourrai, Abdelilah Radi, Jihane El Mahi, Ghita Hachim
Publikováno v:
Journal of Advances in Medical and Pharmaceutical Sciences. :8-13
Hyper-IgE syndrome (HIES) is a primary immunodeficiency disorder characterized by eczema, cold abscesses, pneumonia, eosinophilia, and a very high serum IgE concentration. An association with celiac disease is rare. Immunodeficiency and autoimmunity