Cystic fibrosis liver disease.
Cystic fibrosis (CF) is an inherited autosomal recessive disease that affects exocrine systems including sinuses, lungs, pancreas, liver, skin, gastrointestinal tract, and reproductive tract. The effects on the liver ranges from elevated liver function tests to cirrhosis and liver failure. The labor...
| Publicado en: | Journal of Pain Management Vol. 16; no. 3; pp. 195 - 216 |
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| Autor principal: | |
| Formato: | tables/charts Journal Article |
| Publicado: |
Nova Science Publishers, Inc.
2023
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=176626440&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 176626440 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 19395914 903P jtl: Journal of Pain Management issn: 19395914 maglogo: N pubinfo: dt: 2023 vid: 16 iid: 3 pid: 1040 pub: Nova Science Publishers, Inc. place: Hauppauge, New York artinfo: ui: 176626440 176626440 176626440 176626440 ppf: 195 ppct: 21 formats: fmt: @attributes: type: P tig: atl: Cystic fibrosis liver disease. aug: au: Barr, Jayne A. affil: Internal Medicine, Department of Internal Medicine, MetroHealth Case Western Reserve University, Cleveland, Ohio, USA sug: subj: Cystic Fibrosis Liver Diseases Lung Diseases Pancreas Pathology Skin Diseases Gastrointestinal System Pathology Genital Diseases Liver Transplantation Quality of Life Quality Improvement Life Expectancy ab: Cystic fibrosis (CF) is an inherited autosomal recessive disease that affects exocrine systems including sinuses, lungs, pancreas, liver, skin, gastrointestinal tract, and reproductive tract. The effects on the liver ranges from elevated liver function tests to cirrhosis and liver failure. The laboratory and radiographic screening, treatment alternatives, and organ transplantation are important aspects in the care of CF patients. Liver transplant and lung-liver transplant can improve the quality of life and life expectancy. Optimal timing for referral for liver transplantation remains controversial. Future research of cystic fibrosis liver disease continues to focus on the CFTR defect, genetic modifiers, and the biliary bicarbonate exchange. pubtype: Academic Journal doctype: tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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