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cftr nejm peds annual bmj clinical diagnosis dios distalintestinalobstructionsyndrome ebm education foam im ivacaftor kub management modulatortherapy mutations nice pathophys
Cystic Fibrosis An autosomal recessive condition. Mutations affect a specific gene on chromosome 7. The affected
#CysticFibrosis
Monitoring people with cystic fibrosis #Screening #Management #Peds #PrimaryCare #CysticFibrosis #Screening #Annual #NICE #BMJ
#PrimaryCare #CysticFibrosis
Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del #EBM #CysticFibrosis #Tezacaftor #Ivacaftor #CFTR #Phe508del #NEJM
Phe508del #EBM #CysticFibrosis
The Cribsiders episode: "Cystic Fibrosis Licked-ty Split with Dr. Whittney Warren" #cysticfibrosis #cftr #pediatrics #podcast #education
Whittney Warren" #cysticfibrosis
Distal Intestinal Obstruction Syndrome (DIOS), previously known as “meconium ileus equivalent,” is an entity unique to
Radiology #KUB #DIOS #CysticFibrosis
Classes of Mutations in the Gene Encoding Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). Depending on the
Pathophys #Pulm #Peds #CysticFibrosis
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