Data in Brief (Dec 2018)
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score
- Philippe Moulin,
- Robert Dufour,
- Maurizio Averna,
- Marcello Arca,
- Angelo B. Cefalù,
- Davide Noto,
- Laura D’Erasmo,
- Alessia Di Costanzo,
- Christophe Marçais,
- Luis Antonio Alvarez-Sala Walther,
- Maciej Banach,
- Jan Borén,
- Robert Cramb,
- Ioanna Gouni-Berthold,
- Elizabeth Hughes,
- Colin Johnson,
- Xavier Pintó,
- Željko Reiner,
- Jeanine Roeters van Lennep,
- Handrean Soran,
- Claudia Stefanutti,
- Erik Stroes,
- Eric Bruckert
Affiliations
- Philippe Moulin
- Hôpital Cardiovasculaire Louis Pradel, Hospices Civils de Lyon, INSERM UMR 1060 Carmen, Université Claude Bernard Lyon 1, Lyon, France
- Robert Dufour
- Institut de Recherches Cliniques de Montréal, Montréal, Canada
- Maurizio Averna
- Dipartimento Biomedico di Medicina Interna e Specialistica (Di.Bi.M.I.S.), University of Palermo, Palermo, Italy
- Marcello Arca
- Department of Internal Medicine and Medical Specialties, Sapienza University of Rome, Rome, Italy
- Angelo B. Cefalù
- Dipartimento Biomedico di Medicina Interna e Specialistica (Di.Bi.M.I.S.), University of Palermo, Palermo, Italy
- Davide Noto
- Dipartimento Biomedico di Medicina Interna e Specialistica (Di.Bi.M.I.S.), University of Palermo, Palermo, Italy
- Laura D’Erasmo
- Department of Internal Medicine and Medical Specialties, Sapienza University of Rome, Rome, Italy
- Alessia Di Costanzo
- Department of Internal Medicine and Medical Specialties, Sapienza University of Rome, Rome, Italy
- Christophe Marçais
- Hôpital Cardiovasculaire Louis Pradel, Hospices Civils de Lyon, INSERM UMR 1060 Carmen, Université Claude Bernard Lyon 1, Lyon, France
- Luis Antonio Alvarez-Sala Walther
- Hospital General Universitario Gregorio Marañón, IiSGM, Department of Medicine, School of Medicine, Universidad Complutense de Madrid, Madrid, Spain
- Maciej Banach
- Medical University of Lodz, Lodz, Poland
- Jan Borén
- University of Gothenburg, Gothenburg, Sweden
- Robert Cramb
- University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK
- Ioanna Gouni-Berthold
- University of Cologne, Cologne, Germany
- Elizabeth Hughes
- Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK
- Colin Johnson
- University Hospital, Southampton, UK
- Xavier Pintó
- Bellvitge University Hospital, Barcelona, Spain
- Željko Reiner
- University Hospital Center Zagreb, Zagreb, Croatia
- Jeanine Roeters van Lennep
- Erasmus Medical Centre, Rotterdam, the Netherlands
- Handrean Soran
- Central Manchester University Hospital NHS Foundation Trust, Manchester, UK
- Claudia Stefanutti
- Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy
- Erik Stroes
- Academic Medical Center, Amsterdam, the Netherlands
- Eric Bruckert
- Endocrinologie Métabolisme et Prévention Cardiovasculaire, Institut E3M et IHU Cardiométabolique (ICAN), Hôpital Pitié Salpêtrière, 47–83 Boulevard de l’Hôpital, 75013 Paris, France; Corresponding author.
- Journal volume & issue
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Vol. 21
pp. 1334 – 1336
Abstract
Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.
