Cystic Fibrosis PPT课件
Cystic Fibrosis Gene Mutations and Pancreatitis Risk Relation… 热度: Vitamin D Deficiency Is Associated with Pulmonary Exacerbations in Children with Cystic Fibrosis 热度: CysticFibrosisCysticFibrosis MarieMarie--MartineLogvinoff,M.D.MartineLogvinoff,M.D. ...
1938:Cysticfibrosis •DorothyHAndersen •1901-1963 •anieceofHansChristianAndersen. •Shewasabrightcompassionate andsensitivescientistwhowasalso achainsmokeranddiedoflung cancerattheageof62years. •Eventuallyover600childrenwith CFwerereferredtoherinNew ...
The goals of cystic fibrosis treatment are to: Prevent and control lung infections Loosen and remove thick, sticky mucus from the lungs, prevent or treat blockages in the intestines, provide enough nutrition, Prevent dehydration (a condition in which the body doesn't have enough fluids) Living ...
囊性纤维病抗生素的应用(英文课件)Inhaled Antibiotics in Cystic Fibrosis.ppt,教学课件课件PPT医学培训课件教育资源教材讲义Inhaled Antibiotics in Cystic Fibrosis;Case Presentation;Case Presentation;Case Presentation;Case Presentation;Case Presentation;Case Pr
•1988–Geneiscloned:1000mutationsin 2005 CysticFibrosis •CFisdiseaseofexocrineglands,withmulti •••••• organinvolvementAutosomalrecessive……….chromosome7.Variablemanifestations.1/3500whitelivebirthsinUSMediansurvivalis30yearsNocureResistanttoTB,cholera CFTR •DeltaF508,phenylalaninedeletion...
CysticFibrosisFoundation.ClinicalPracticeGuidelinesforCysticfibrosis.1997.Welsh,MJandSmith,AE.CysticFibrosis.ScientificAmerican.273(6):52,1995.BurdenofCF BurdenofCF(continued)CFSurvival AutosomalrecessiveinheritanceinCF LetC=normalCFTRLetc=mutantCFTRIfmomanddadarebothcarriersthen:CCCCcCc Withmomanddad...
Evaluation of bronchial constriction in children with cystic fibrosis after inhaling two different preparations of tobramycin. OBJECTIVES: This randomized, double-blind, cross-over study evaluated the risk of bronchoconstriction with two preparations of inhaled tobramycin in childr... GA Alothman,MM Alsa...
Cigarette smoke, well-known to be the major cause of COPD, contributes to suppression of the expression and function of cystic fibrosis transmembrane conductance regulator protein. Likewise, there is evidence that cystic fibrosis transmembrane conductance...
Anne K. SwisherLinda BaerKathryn MoffettRachel YeaterCardiopulmonary Physical Therapy JournalSwisher AK, Baer L, Moffett K. The influence of lean body mass and leg muscle strength on 6-minute walk test performance in children with cystic fibrosis. Cardiopulm Phys Ther J. 2005...