About: Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie

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About: Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie
Creator	Caquard, M Parlier, G Siret, D
Source	Elsevier; PMC
abstract	This article presents the clinical observation of 2 cases of children suffering from Kawasaki disease in the same family at a 7-year interval. This observation suggests a genetic predisposition to the disease. Epidemiological surveys conducted in Japan for some years point to a genetic factor but without proof. Childhood systemic febrile vasculitis is hard to recognise, so its diagnosis is often made lately, while there is an effective therapy, which prevents from serious cardiovascular complications. Identification of its precise cause, a necessary step before any diagnostic laboratory test, will be a major breakthrough.
has issue date	2006-04-21(xsd:dateTime)
bibo:doi	10.1016/j.arcped.2006.02.012
bibo:pmid	16630711
has license	no-cc
sha1sum (hex)	5558b9b15a0a761b7e4ea495f5432d53cfdc13cd
schema:url	https://doi.org/10.1016/j.arcped.2006.02.012
resource representing a document's title	Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie
has PubMed Central identifier	PMC7118996
has PubMed identifier	16630711
schema:publication	Arch Pediatr
resource representing a document's body	covid:5558b9b15a0a761b7e4ea495f5432d53cfdc13cd#body_text
is schema:about of	named entity 'internet' named entity 'FAMILY' named entity 'OBSERVATION' named entity 'SISTER' named entity 'ACCEPT' named entity 'CASES' named entity 'KAWASAKI' named entity 'MALADIE' named entity 'BROTHER' named entity 'UNE' named entity 'CAS' named entity 'INTERNET' named entity 'KAWASAKI DISEASE' named entity 'SUR' named entity '2006' named entity '2006' named entity 'cases' named entity 'Kawasaki disease' named entity 'à propos' named entity 'dont' named entity 'mois' named entity 'leucocytes' named entity 'aspirine' named entity 'Le bilan' named entity 'leucocytes' named entity 'la 1' named entity '3,5' named entity 'ceftriaxone' named entity 'mois' named entity 'dont' named entity 'Cette' named entity 'mois' named entity 'leucocytes' named entity 'HLA' named entity 'aspirine' named entity 'mis' named entity 'aspirine' named entity 'ceftriaxone' named entity 'le bilan' named entity 'Kawasaki' named entity 'sur' named entity '2005' named entity 'cas' named entity 'Family' named entity 'dans' named entity 'disease' named entity 'observation' named entity 'de 2'
is part of of	covid:5558b9b15a0a761b7e4ea495f5432d53cfdc13cd#body_text This article presents the clinical observation of 2 cases of children suffering from Kawasaki disease in the same family at a 7-year interval. This observation suggests a genetic predisposition to the disease. Epidemiological surveys conducted in Japan for some years point to a genetic factor but without proof. Childhood systemic febrile vasculitis is hard to recognise, so its diagnosis is often made lately, while there is an effective therapy, which prevents from serious cardiovascular complications. Identification of its precise cause, a necessary step before any diagnostic laboratory test, will be a major breakthrough. Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie

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