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Artikel ; Online: Classic Cystic Fibrosis Presentation in Two Middle Eastern Siblings with a rare CFTR mutation (c.80G>T)

Sumaiya Hafiz / Sarah Al Qassimi / Ali Saeed Wahla / Mahmoud El-Kaissi / Mateen Uzbek / Irfan Shafiq

European Journal of Case Reports in Internal Medicine (2023)

2023  

Abstract: Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across ... ...

Abstract Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across the cell membrane. We describe the cases of two siblings with CF diagnosed with the rare missense mutation c.80G>T, which has only been referenced once in the literature and shows a possible association with classical form of CF.
Schlagwörter cystic fibrosis ; middle east ; cftr mutation ; c.80g>t ; Medicine ; R
Sprache Englisch
Erscheinungsdatum 2023-02-01T00:00:00Z
Verlag SMC MEDIA SRL
Dokumenttyp Artikel ; Online
Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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