Article (Scientific journals)
Comment j’explore. Une macrocéphalie.
Vanden Brande, Laura; ALKAN, Serpil; BARREA, Christophe et al.
2022In Revue Médicale de Liège, 77 (1), p. 56-62
Peer reviewed
 

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Keywords :
Child; Humans; Megalencephaly/diagnosis; Hydrocephaly; Megalencephaly; Paediatric; Macrocephaly
Abstract :
[en] Macrocephaly is a frequent reason for seeking advice in a pediatric neurology consultation. It is a non-specific neurological sign that can be isolated, be the sign of a serious acquired pathology or be part of a syndromic picture. Clinical history, physical examination and imaging are key elements of the diagnostic strategy. Signs of intracranial hypertension require an emergency work-up. Genetics, exome in particular, has enabled the characterization of various syndromes associating macrocephaly and neurodevelopmental delay. In this article, we propose an update of practices based on clinical signs.
Disciplines :
Pediatrics
Neurology
Author, co-author :
Vanden Brande, Laura ;  Centre Hospitalier Universitaire de Liège - CHU > Département de Pédiatrie > Service de pédiatrie
ALKAN, Serpil ;  Centre Hospitalier Universitaire de Liège - CHU > Département de Pédiatrie > Service de pédiatrie
BARREA, Christophe  ;  Centre Hospitalier Universitaire de Liège - CHU > Département de Pédiatrie > Service de pédiatrie
LEROY, Patricia ;  Centre Hospitalier Universitaire de Liège - CHU > Département de Pédiatrie > Service de pédiatrie
Language :
French
Title :
Comment j’explore. Une macrocéphalie.
Alternative titles :
[en] How I explore... macrocephaly
Publication date :
January 2022
Journal title :
Revue Médicale de Liège
ISSN :
0370-629X
eISSN :
2566-1566
Publisher :
Université de Liège. Revue Médicale de Liège, Liège, Belgium
Volume :
77
Issue :
1
Pages :
56-62
Peer reviewed :
Peer reviewed
Available on ORBi :
since 21 January 2022

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