A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency.

Vitali, Cecilia; Bajaj, Archna; Nguyen, Christina; Schnall, Jill; Chen, Jinbo; Stylianou, Kostas; Rader, Daniel J; Cuchel, Marina

Vitali, Cecilia; Bajaj, Archna; Nguyen, Christina; Schnall, Jill; Chen, Jinbo; Stylianou, Kostas; Rader, Daniel J; Cuchel, Marina.

Afiliação

Vitali C; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Bajaj A; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nguyen C; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Schnall J; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Chen J; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Stylianou K; Department of Nephrology, Heraklion University Hospital, Crete, Greece.
Rader DJ; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Cuchel M; Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: mcuchel@pennmedicine.upenn.edu.

J Lipid Res ; 63(3): 100169, 2022 03.

Article em En | MEDLINE | ID: mdl-35065092

Assuntos

Deficiência da Lecitina Colesterol Aciltransferase; Humanos; Biomarcadores; Heterozigoto; Deficiência da Lecitina Colesterol Aciltransferase/complicações; Deficiência da Lecitina Colesterol Aciltransferase/genética; Mutação; Fosfatidilcolina-Esterol O-Aciltransferase/genética

Palavras-chave

HDL; chronic kidney disease; esterified cholesterol; familial LCAT deficiency; fish-eye disease; human data; lecithin:cholesterol acyltransferase; nephrotic syndrome; proteinuria/hematuria; systematic review

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência da Lecitina Colesterol Aciltransferase Tipo de estudo: Observational_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: J Lipid Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

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