نتایج جستجو برای: familial chylomicronemia
تعداد نتایج: 56099 فیلتر نتایج به سال:
normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 colorectal cancer is classified in to three forms: sporadic (70-75%), familial (20-25%) and hereditary (5-10%). hereditary colorectal cancer syndromes classified into two different subtypes: polyposis and non polyposis. familial adenomatous polyposis (fap; omim #175100) is the most common polyposis syndrome, account for <1...
familial hypercholesterolemia (fh) is an inherited common autosomal mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in 500. fh is characterized by severely elevated levels of low-density lipoprotein cholesterol (ldl-c), which result in surplus deposition of cholesterol in tissues. this condition leads to premature at hero sclerosis and early-onset of coronary hear...
cronkhite-canada syndrome (ccs) is a rare, non-familial disorder of unknown etiology associated with alopecia, cutaneous hyperpigmentation, gastrointestinal polyposis, onychodystrophy, diarrhea, weight loss and abdominal pain.the prevalence ofâ gastrointestinal malignancy in ccs patients is about 13%, and especially is high in colorectal and gastric areas; 5 year mortality rate is 55%. in this ...
introduction: the objective of the present study is to investigate the relationship between the familial history of digestive system cancers and development of gastric cancer. methods: in this case-control study conducted in 2012, 84 patients with a definite diagnosis of gastric cancer, diagnosed using endoscopy and pathological study of biopsies, were compared with 84 people with the same age ...
background hepatitis c virus (hcv) is a major cause of chronic liver disease worldwide. the role of intra familial hcv transmission is still controversial. the aim of the present study is to determine intra familial transmission (sexual and non sexual contacts) of hcv in a group of iranian population. patients and methods in this historical cohort study, 270 first degree relatives of hepatitis ...
background since genetic and most environmental factors shape the context of families, some studies have been initiated to investigate the role of familial relationships in metabolic syndrome (mets). objectives to estimate the familial aggregation of mets and its components by identifying both case and control probands among tehranian adults with different socio-behavioral and reproductive char...
introduction dilated cardiomyopathy (dcm) is the leading cause of heart failure and arrhythmia. case presentation a 47-year-old male, diagnosed with dilated cardiomyopathy, died due to heart failure. during the screening of his family members, his 17-year-old daughter and 9-year-old son also had dilated cardiomyopathy. another daughter had died suddenly at the age of 12 years. conclusions we he...
Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder characterized by increased levels of total cholesterol and low density lipoprotein cholesterol. The FH clinical phenotype has been associated with increased risk of coronary heart disease and premature death. The mutation in LDLR gene in most cases is responsible for FH phenotype. Furthermore, other ...
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