Zobrazeno 1 - 10
of 34
pro vyhledávání: '"R. El Qadiry"'
Publikováno v:
Case Reports in Endocrinology, Vol 2022 (2022)
Turner’s syndrome (TS) is a sex chromosome disorder due to loss of either all or part of the X chromosome, in some or all the cells of the body. Neurofibromatosis type 1 (NF-1) is a multisystemic genetic disorder that is only rarely observed in ass
Externí odkaz:
https://doaj.org/article/8a83378a33c7424ca8680233fe56db58
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Pituitary stalk interruption syndrome (PSIS) is a very rare entity, and the clinical manifestations are nonspecific. Neonatal cholestasis due to endocrine disorders is rare and poorly recognized. Our case report describes a case of PSIS in a Moroccan
Externí odkaz:
https://doaj.org/article/33954f3d3dfe4c6d94c49229f827d3ec
A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastr
Externí odkaz:
https://doaj.org/article/4a16687c5ee14d07bc8af5004e1cd53e
Publikováno v:
Rheumatology. 61
Background Behçet disease is a rare vasculitis that involves medium and small calibre arteries. Multisystem involvement is possible. Few are the papers that provide information about its clinical course, and outcome in the pediatric population. Also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa6825ebb662811cb6234276027d91a2
https://doi.org/10.1093/rheumatology/keac496.056
https://doi.org/10.1093/rheumatology/keac496.056
Publikováno v:
Rheumatology. 61
Background Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease that can involve any organ system with a wide range of disease manifestations, and can lead to significant morbidity and even mortality. Objectives To describe the epidemio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d642946a97bb389474b1ad21b59d805c
https://doi.org/10.1093/rheumatology/keac496.041
https://doi.org/10.1093/rheumatology/keac496.041
Publikováno v:
Scholars Journal of Medical Case Reports. 9:1066-1068
Celiac disease is an autoimmune enteropathy related to gluten intolerance that can have several neurological complications, including cerebellar ataxia. The mechanism involved remains poorly understood. The gluten-free diet is the mainstay of therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb0b84fa821e4cfe4adaa5c1d55e386
https://doi.org/10.36347/sjmcr.2021.v09i11.006
https://doi.org/10.36347/sjmcr.2021.v09i11.006
Autor:
R, El Qadiry1 (AUTHOR) Rabiy.elqadiry@gmail.com, A, Lalaoui1 (AUTHOR), H, Nassih1 (AUTHOR), I, Aitsab1 (AUTHOR), A, Bourrahouat1 (AUTHOR)
Publikováno v:
Clinical Medicine Insights: Case Reports. 1/13/2021, p1-3. 3p.
A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
Case Reports in Pediatrics
Case Reports in Pediatrics
Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad58584da6bacc2b92e5e77aa65bf2bc
https://doaj.org/article/4a16687c5ee14d07bc8af5004e1cd53e
https://doaj.org/article/4a16687c5ee14d07bc8af5004e1cd53e
Publikováno v:
The Open Infectious Diseases Journal. 10:142-146
Introduction: Newborn cellulitis is rare and often atypical disease. It is a diagnostic and therapeutic emergency and its progress leads to instant death. We report three cases of neonatal cellulitis from the Neonatal ICU Department of Mohammed VI un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf99a4185b39b15fc40f54bc8ebdd964
https://doi.org/10.2174/1874279301810010142
https://doi.org/10.2174/1874279301810010142
Publikováno v:
The Open Infectious Diseases Journal. 10:139-141
Introduction: Sickle cell disease is a haemoglobinopathy characterized by the occurrence of vaso-occlusive crises and osteoarticular complications. Case-Report: We report the case of an infant with sickle cell disease revealed by a bilateral abscess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c227fd6aa7be0993cbca29edb2804bba
https://doi.org/10.2174/1874279301810010139
https://doi.org/10.2174/1874279301810010139