نتایج جستجو برای: weils syndrome
تعداد نتایج: 621915 فیلتر نتایج به سال:
results; out of 634 patients, 61 subjects (9.62%) had significant complications including: acute renal failure, alveolar hemorrhage, ards, clotting disorders, pancreatitis, gastrointestinal bleeding and intracranial bleeding; age, jaundice, renal and pulmonary involvement (oliguria and anuria), hypotension, leukocytosis, thrombocytopenia, hyponatremia, elevated bilirubin, alanine aminotransfera...
a 3.5 month-old girl was admitted with silvery gray hair, light colored skin, recurrent diarrhea, chest infections, hepatosplenomegaly, episodes of pancytopenia, and hemophagocytosis in the bone marrow. light microscopy of hair showed characteristic large and irregular clumps of melanin in the middle of hair shaft. peripheral blood smear examination did not show giant granules in granulocytes....
objectives the aim of this study was to evaluate the effect of cranberry extract on some components of metabolic syndrome. patients and methods in a randomized, double-blind placebo-controlled clinical trial, 48 obese and overweight females diagnosed with ms were assigned into two groups to receive cranberry supplement or placebo for an eight-week period. serum glucose, lipoproteins, inflammato...
conclusions we showed that patients with metabolic syndrome have larger infarct size compared to control subjects. background infarct size is an important surrogate end point for early and late mortality after acute myocardial infarction. despite the high prevalence of metabolic syndrome in patients with atherosclerotic diseases, adequate data are still lacking regarding the extent of myocardia...
Introduction: Metabolic syndrome is a series of disorders such as central obesity, hypertriglyceridemia, decreasing HDL, abnormal blood glucose and hypertension that ultimately lead to the risk of cardiovascular disease, diabetes and other problems. The aim of this study was to determine the prevalence of this syndrome among adults in Yazd. Methods: This study was performed using the data of t...
Sjogren-Larsson Syndrome (SLS) is an inherited autosomal recessive neurocutaneous disorder with congenital ichthyosis, spastic diplegia or quadriplegia and mental retardation. We report a case of Sjogren-Larsson Syndrome with clinical profile (mental retardation, ichthyosis, spastic diplegia) and MRI findings such as seen in multiple sclerosis (MS). So this rare syndrome can be another differen...
keratoderma is a group of disorders characterized by abnormal thickening of skin. acquired palmar keratoderma has many underlying causes. the association of thyroid disease and palmar keratoderma rarely reported. hypothyroidism, although very rare association, must be suspected in patients with acquired ppk, particularly when it occurs in setting of systemic symptoms or predisposing conditions....
abstract a 2.5 year old girl is presented with both hands constriction bands leading to distal amputations and the rare deformity of shoulder duplication in the right side accompanying constriction skin marking over the affected shoulder. the cephalomedial scapula articulated with the clavicle and the caudolateral scapula articulated with humeral head. the most important physical finding which ...
conclusions the frequency of rls among our patients was remarkable and we conclude that all patients who are undergoing hemodialysis should be screened for rls, which can assist in providing proper attention and treatment. results according to our results, 54.5% of patients were diagnosed with rls, and of those 65.2% and 42.9% were women and men, respectively. rls is seen more often among patie...
purpose: to report two sisters with congenital myasthenic syndrome (cms) masquerading as myasthenia gravis. patients and findings: two six and seven years old sisters presented with variable strabismus, ptosis, and fatigue. all symptoms were aggravated with exercise and improved with rest. intramuscular prostigmin injection decreased their symptoms. a diagnosis of cms was made according to earl...
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