نتایج جستجو برای: case report
تعداد نتایج: 1843127 فیلتر نتایج به سال:
Malformations which occur during the development of the avian body organs can lead to structural and functional abnormalities. Most defects are recognized at hatching, but some go undetected until somewhat later. The cause of the majority of animal congenital malformations is unknown. A significant proportion of congenital malformations of unknown cause are likely to have an important genetic c...
BACKGROUND AND AIM: Surgical endodontics may sometimes fail despite using root-end filling materials (REFMs). In this case report, a symptomatic right maxillary first premolar underwent periradicular surgery (PS) for replacing huge rate of amalgam with mineral trioxide aggregate (MTA).CASE REPORT: A thirty-year-old healthy woman attended with the chief complaint of recurrent swelling and absces...
Background Maple Syrup Urine Disease (MSUD) is a rare autosomal recessive metabolic error, characterized by Branched Chain α-Keto-acid Dehydrogenase Complex (BCKDC) deficiency. Mutations in 3 genes can lead to abnormal metabolism and accumulation of leucine, isoleucine, valine and corresponding keto-acids. MSUD affects 1 in 185,000 infants globally. Seizure is a common presentation among neonat...
This technical report provides a theoretical basis for the implementation of a TTCN test case simulator. In order to base the implementation on existing code, an automata based model has been chosen, i.e., in the model a TTCN test case shows an automaton like behavior. The procedure is the following: TTCN test cases are transformed into an internal structure, which afterwards can be interpreted...
In 2002, Thailand achieved universal health coverage through the introduction of the Universal Coverage Scheme (UCS). However, people with citizenship problems, so-called 'stateless people', were left uninsured. Consequently, the 'Health Insurance for People with Citizenship Problems' (HIS-PCP) policy was adopted in 2010 with features emulating the UCS. This study sought to examine the operatio...
This was Presented in 5th International Congress of Iranian Iranian Society of Knee Surgery, Arthroscopy, and Sports Traumatology (ISKAST), 14-17 Feb 2018- Kish, Iran
Introduction: Retropharyngeal lipoma is a rare benign tumor (less than 27 reports in literature) of nonspecific clinical symptoms. It can grow to an enormous extent causing total obstruction of the upper respiratory tract. Until now its etiology is unknown. Case Report: A 60-year old female complained from severe snoring mild dysphagia and moderate respiratory difficulty with gradual onset si...
Holoprosencephaly (HPE) is a rare congenital brain malformation associated with multiple midline facial defects. This anomaly is resulted from the failure of diverticulation and cleavage of primitive prosencephalon during weeks 4-8 of gestation. HPE is the most common forebrain developmental anomaly in human with the incidence rate of 0.49-1.2 cases per 10,000-20,000 term births. In this study,...
A rare case of splenic harmartoma in a 31 year old female is reported. She was admitted with splenomegaly, fever and chronic history of epistaxis. Routine hematological survey revealed pancytopenia and mild hypercellular marrow. Abdominal sonography showed a space-occupying lesion in the spleen which was suspected as malignant tumor. Splenectomy was performed and histologic findings were d...
Abstract Familial hypercholesterolemia (FH) is a hereditary dislipidemia. Patients present with extremely high level of low-density lipoprotein cholesterol (LDL-C), which is due to mutation in the gene of LDL receptor. Homozygous patients (HoFH) whose incidence is 1 in 1.000.000 are at high risk of premature aortic valve stenosis, and coronary artery atherosclerosis. In homozygous individual...
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