Tibiocalcaneal arthrodesis using screws in the treatment of equinovarus deformity of the foot in adult: a retrospective study of 42 cases
The authors have retrospectively studied 42 cases of tibiocalcaneal arthrodesis using large cannulated AO screws, staples and iliac crest graft mixed in treatment of fixed equinovarus deformity of the foot in adult patients. There were 25 men and 17 women aged 22 to 70 (mean, 45) years. All patients were reviewed with an average of 5 years. The operations were performed between 2005 and 2012.Preoperatively, all patients had 50° of the mean calcaneal varus deformity and 75° (60-90°) of equinus deformity on Meary’s radiological. There were 24 idiopathic, 8 post traumatic,6 neurologic associated with IMC,4 polio. Clinical and functional outcome was assessed with the kitaoka score, the x-rays included an AP and lateral view of the ankle and Meary view .Resultats were excellent in 73% , good in 18 % , fair in 9%. X-rays showed 3 nonunions after 2 years and were reported. We noted 2 postoperative cutaneous necrosis; the shortening was an average 2 cm. After a mean follow-up duration of 5±2.93 years; All patients stated that they improvement of pain and function. 40 patients returned to independent ambulation, wearing custom-made shoes with molded insoles. We belive that the tibiocalcaneal arthrodesis should be used to treat the fixed equinovarus deformity in the adult whatever its etiology.
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“Coarctation of aorta”- embryological basisand its clinical significance.
The term Coarctation can be defined as the stricture or narrowing of the aorta, it affects both child and adult, but is seen mostly in children. Coarctation can be either be preductal or postductal. Depending on the severity of the condition and the time of diagnosisthe treatment can be determined in an individual.Identifying this condition very early in life is also beneficial to the patient even though there would be a few complications that would be faced depending on the form of treatment one choses. The present study aimed to understand the embryological basis and its clinical significance.
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A mathematical model of two phase Newtonian layered renal blood flows in capillaries remote from the heart and proximate to the kidney with special reference to Diabetes
In the present paper we have formulated the renal blood flow along the capillaries in case of renal disease Diabetes . keeping in the view the nature of renal circulatory system in human body. P.N.Pandey and V.Upadhyay have considered the blood flow has two phased one of which is that of red blood cells and other is plasma. According to Fahreaus-Lindqvist effect the blood flow in two separated layers while passing through capillaries. The plasma layer which flows along the surface of the capillaries contains almost no blood cells. The second layer the core layer containing blood cells which flows in plasma along the axis of capillary. We have collected a clinical data in case of Diabetes for hematocrit v/s blood pressure. The graphical presentation for particular parametric value is much closed to the clinical observation. The overall presentation is in tensorial form and solution technique adapted is analytical as well as numerical. The role of hematocrit is explicit in the determination of blood pressure drop in case of renal disease Diabetes
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Arrhythmia and chronic kidney disease
Cardiac involvement is the leading cause of death in patients with chronic kidney disease (CKD), including cardiac arrhythmias that increase the risk of sudden death. The purpose of our work is to study the prevalence of heart complications in this population and to propose better cardiac and nephrological management.A total of 92 patients with CKD participated in the study, in the Department of Renal Dialysis and Renal Transplantation the Mohammed V Military Training Hospital in Rabat, the mean age of the patients was 50 years ± 16.55 with extremes ranging from 34 to 76 years, sex ratio was 1.1(H / F). Causal nephropathy is indeterminate in 48% of cases, 58% of our patients are hypertensive; 64% had cardiac arrhythmias; the electrical abnormalities were respectively: left ventricular hypertrophy in 41,4% of cases, left atrial hypertrophy in 9,2 % of cases, atrial fibrillation in 5,5 % of cases and repolarization disorders respectivelyin 12 % of cases.
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CT angiographically demonstrated variation in origin of inferior phrenic arteries in asian population and its clinical implication with review of literature
The lack of ample amount of literature, limited size of the study group in the available studies and relating the potential clinical applications of variation of origin of inferior phrenic artery has validated the study so that additional information could be added to the present literature. Objective: Few dedicated studies have been available demonstrating variations in the origin of inferior phrenic in the present growing era of intervention radiology. The cause has been satisfied by studying a group of 100 patients and reviewing the available literature. Methods: A group of 100 patients that were the potential liver and renal donors were studied in a 40 slice CT scanner as pre transplant evaluation in the Department of Radiology, Institute of nuclear medicine and allied sciences ,Timarpur ,New Delhi. Results: The right inferior phrenic arteries arise from abdominal aorta in 41(42%) of cases, celiac axis 50(50%) ,right renal artery 7(7%) and from left gastric in 2(2%) of cases. The left inferior phrenic arise from aorta in 38(38%) of cases, celiac axis in 55(52%) of cases, left renal artery 4(4%),left gastric artery in 3(3%) of cases. Conclusion: The importance of the IPA is not limited to the arterial supply to the diaphragm . Practically any hepatic neoplasm (including metastatic disease to the liver) may receive blood supply from the IPA. Literature have been reviewed regarding variation in origin of inferior phrenic artery and its implication in surgical intervention. KEYWORDS: Inferior phrenic artery, diaphragm
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Efficacy of Urotensin II in Cardiovascular System
Cardiovascular diseases (CVDs), including coronary arter disease, cerebrovascular events, rheumatic heart disease and arter diseases, remain the most common cause of death in the world. Changes in the regulation of vasoactive peptides in abnormal conditions, cardiovascular diseases; Endothelial dysfunction, which is the critical processes underlying vascular damage, results in vascular repair and inflammation. Studies with specific receptor antagonists; It will be very important to understand the physiological role of urotensin II and its receptor and to reveal its therapeutic potential. The aim of this study is to know the pathophysiological role of U-II following the development of UT receptor antagonists and to give an insight into the design of new drugs and to give a current perspective. The development of urotensin receptor antagonists may provide a useful diagnosis tool as well as a new treatment for cardiovascular diseases.
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Epilepsy in children and imaging: About thirty cases
Epilepsy is a chronic condition that often begins in childhood and is characterized by the occurrence of spontaneous and recurrent epileptic seizures. The aim of our study is to identify the different etiologies of epilepsy in children and to highlight the importance of imaging in the etiological diagnosis, in the extension assessment and in the therapeutic management of epilepsy. Our study was carried out over a 5-year period from January 2014 and 2019, and involved 30 cases in the pediatric radiology department of the Rabat Children's Hospital. Seizures and loss of consciousness dominated the clinical picture. The etiological diagnosis in the majority of our series was based on CT scan and brain magnetic resonance imaging. The evolution under treatment was favourable for all our patients.
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178. Freeman-Sheldon Syndrome: About a rare observation |
Jawad Lahma, Sondos Al Rajab, Zakaria Arkoubi, Reda Hejjouji, Sophia Nitassi, Ali El Ayoubi, Razika Bencheikh, Mohammed Anas Benbouzid, Abdelilah Oujilal and Leila Essakalli |
Abstract |
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Category : Medical Sciences | Sub Category : Physiology and Anatomy |
Freeman-Sheldon Syndrome: About a rare observation
Freeman-Sheldon Syndrome (FSS), also known as Distal Arthrogryposis Type 2A (DA2A), Craniocarpotarsal Dystrophy, Windmill-Vane-Hand Syndrome, or Whistler Face Syndrome, was first described by Freeman and Sheldon in 1938 [1,2]. It is a very rare syndrome of multiple congenital contractures characterized by a microstomy giving the appearance of the "whistling face", a club foot and articular contractures. FSS is the most severe form of distal arthrogryposis. We report a rare observation of a two years old child, who has a poly malformative syndrome admitted in our ENT department at the Specialty Hospital, Rabat. On examination, the child presents a facial dysmorphism with head bird facies with prominent forehead, hyperthelorism and small mouth. Otherwise, H aspect of the chin and mandibular retrognation are noted. At the endoral examination, we notice a cleft palate, dental overlap and glossoptosis. Moreover, osteo-articular examination shows hypertonicity of the limbs, especially on the fingers, and a left club foot. The geneticist's opinion is in favor of a Freeman-Sheldon syndrome. The child has benefited from a surgical closure of the cleft palate. FSS is caused by genetic abnormalities involving the "distal arthrogryposis multiplex congenita" gene, whose inheritance may be either mostly autosomal dominant or autosomal recessive. The management by health professionals of several medical disciplines must be undertaken from birth to evaluate the severity of their phenotypic presentation and minimize the risk of patient development delay.
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Mapping the Cohesion and Synergy in Clinical Research Sites
Clinical research competencies are enhanced when there is synergy and strong internal cohesion, with the appropriate level of clinical expertise in recruitment of participants and undertaking a study from initial stages, to conclusion. When a study sponsor approaches a site to conduct a clinical trial, the site must convey accurately that it has the resources and capability to undertake a study. The clinical research site should be able to demonstrate competencies in meeting minimum clinical and research capabilities in conducting a study. Explicit and optimal utilization of available resources and capabilities to meet clinical, regulatory, ethical, and other mandates will reflect this capability. The United States Food and Drug Administration regulatory process is demanding, exacting, time consuming and complicated. Clinical research sites must conform to regulatory clinical research standards. The interaction and collaboration of researchers in different roles and functions in a clinical research study may necessitate studying the factors that promote or constrain inter-professional synergy. The complex human interplay of many diverse and dedicated professionals, comprising clinical site coordinators, researchers, physicians, and research subjects, engaged in clinical research is not fully understood and merits further study. The aim of this scientific paper is to present research to map and assess human dynamics in a clinical research site, so that the results may contribute to reducing the human factors which constrain clinical research. Clinical research sites must cope with intense scrutiny and copious FDA and other regulations, which often limits clinical discovery, lowers financial success and often impedes successful research execution. The exploratory outlook of a future and recommended research study may be deemed important, to examine the positive and negative factors that may facilitate, or impede internal team cohesion within clinical research sites, using a quantitative method and a descriptive design. A comprehensive description of a research plan and data collection methodology is detailed herewith. A study is recommended herewith, based on a research method and design founded on extensive experience in organizational management, review of pertinent literature, and the best practices in clinical research study management.
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Micropapillary Variant of Urothelial Carcinoma of the bladder: Four case reports and a review of the literature
Micropapillary carcinoma (MPC) of urinary tract is an uncommon histological variant of urothelial carcinoma. It is characterized by an aggressive clinical course, an advanced stage at first presentation and a high metastatic potential. Though MPC shows characteristic microscopic features, there exists interobserver variability and controversies concerning certain aspects of this rare tumor. The aim of our study is to present four cases of MPC treated by radical cystectomy in the Department of Urology, at the University Hospital Center of Rabat Morocco, during the period from January 2014 to December 2017. The clinical and morphological features of this rare and aggressive variant of urinary badder carcinoma, as well as a brief review of the literature are all presented.
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