Zobrazeno 1 - 10
of 40
pro vyhledávání: '"M. Kmari"'
Autor:
F. Z. Jounaid, H. Baidi, S. Azitoune, S. Saghir, R. Abilkassem, A. Hassani, M. Kmari, A. Ourrai, A. Agader
Publikováno v:
Scholars Journal of Medical Case Reports. 11:328-331
Vitamin B 12 has important consequences for hematopoiesis and the central nervous system, its deficiency leads to clinical hematological, neurological and psychiatric manifestations. However, most infants with B12 deficiency are born to women with lo
Publikováno v:
Scholars Journal of Medical Case Reports. 10:1167-1169
Introduction: Lysinuric protein intolerance (LPI) is a metabolic disorder resulting from recessive inherited mutations involving the SLC7A7 gene that control the transport of urea cycle intermediates. Case report: In this study we report a case of a
Autor:
H. Lyatim, S. Azitoun, R. Abilkacem, M. Kmari, M. Yajouri, A. Ourrai, A. Hassani, R. M, A. Agadr
Publikováno v:
Scholars Journal of Medical Case Reports. 10:1095-1097
Hydatid cyst commonly affects liver and lung. Cardiac hydatid cyst is an extremely rare disease, due to the development in the heart of the larval form of Taenia Echinococcus granulosus. The diagnosis of this location is difficult due to the absence
Publikováno v:
Asian Journal of Pediatric Research. :6-9
Background: Orbital cellulitis is a diagnostic and therapeutic emergency, jeopardizing the vital and functional prognosis. This study aimed to analyze the epidemiological, therapeutic and evolutional aspects of orbital cellulitis cases treated at the
Publikováno v:
Asian Journal of Pediatric Research. :17-21
Aortopulmonary window (APW) is an uncommon congenital cardiac malformation, accounting for 0.1% of all congenital cardiac diseases. It is a defect between the ascending aorta and the trunk of the pulmonary artery. Such abnormality may occur as an iso
Publikováno v:
Asploro Journal of Pediatrics and Child Health. 3:48-51
Introduction: Innate deficits in the metabolism or transport of vitamin B12 are exceptional. The main cause of vitamin B12 deficiency in infants is secondary to maternal deficiency. Maternal deficiency can have a vegan diet, low socio-economic level
Publikováno v:
Asian Journal of Pediatric Research. :1-7
Bartter syndrome is an inherited renal tubular disorder caused by a defective salt reabsorption in the thick ascending limb of loop of Henle. It characterized by urinary loss of sodium, potassium, and chloride; hypokalemic metabolic alkalosis; normal
Publikováno v:
Asian Journal of Pediatric Research. :1-6
Alagille syndrome is a multi-systemc genetic disorder with variable phenotypic penetrance that was first described in 1969 by Daniel Alagille.It is characterized by anomalies of the intrahepatic bile ducts, heart, eye and skeleton, which are associat
Publikováno v:
Asian Journal of Pediatric Research. :6-10
We report the case of a female child with congenital isolated malabsorption of folic acid. The patient was referred to our hospital for pancytopenia and a tendency to various infections, but with no neurological disturbances. A bone marrow aspiration
Autor:
Abdelilah Radi, Aomar Agadr, Abdelhakim Ourrai, Nadia Mebrouk, Mohamed Selouti, A. Hassani, Rachid Abilkassem, M. Kmari
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Factor VII (FVII) deficiency is the most common among rare inherited autosomal recessive bleeding disorders. It is a multifaceted disease because of the lack of a direct correlation between plasma levels of coagulation FVII and bleeding manifestation