Unpublished conference/Abstract (Scientific congresses and symposiums)
A case of early infantile onset of potentially treatable encephalopathy
Dauby, Justine; Depierreux, Frédérique; Despineux, Charlotte et al.
2022Belgian Society of Pediatric Neurology - Autumn Meeting: Movement Disorders
Peer reviewed
 

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ABSTRACT-TH-Dauby-Justine_25102022.pdf
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Abstract submitted at the BSPN Autumn Meeting, 2022. Presented by Justine DAUBY on the 21th of October 2022.
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DaubyJustineTHD-congres2022.pdf
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Keywords :
Pediatric Movement Disoders; Tyrosine hydroxylase deficiency; Infantile Onset Encephalopathy; Dystonia; Hypotonia; Oculogyric Crisis; Neurogenetics
Abstract :
[en] Diagnosis of Tyrosine Hydroxylase Deficiency (THD) in a 6 months old baby, its broad phenotypic spectrum and treatment.
Disciplines :
Pediatrics
Neurology
Author, co-author :
Dauby, Justine ;  Centre Hospitalier Universitaire de Liège - CHU > > Service de pédiatrie
Depierreux, Frédérique  ;  Centre Hospitalier Universitaire de Liège - CHU > > Service de neurologie ; Université de Liège - ULiège > Département des sciences cliniques
Despineux, Charlotte;  Centre Hospitalier de Luxembourg > Neuropédiatrie
Donge, Mylène;  Centre Hospitalier de Luxembourg > Neuropédiatrie
Marchese, Antonia ;  Centre Hospitalier de Luxembourg > Neuropédiatrie
Scalais, Emmanuel;  Centre Hospitalier de Luxembourg > Neuropédiatrie
Language :
English
Title :
A case of early infantile onset of potentially treatable encephalopathy
Alternative titles :
[fr] A propos d'un cas d'encéphalopathie traitable du nourrisson
Publication date :
21 October 2022
Number of pages :
9
Event name :
Belgian Society of Pediatric Neurology - Autumn Meeting: Movement Disorders
Event organizer :
BSPN - Dr Tessa Wassenberg
Event place :
Bruxelles, Belgium
Event date :
21 octobre 2022
Peer reviewed :
Peer reviewed
References of the abstract :
SESSION 3: Video round on childhood movement disorders / Monoamine neurotransmitter disorders / Abstract n°9
Available on ORBi :
since 22 October 2022

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