A rare cause of facial nerve palsy in children: Hyperostosis corticalis generalisata (Van Buchem disease). Three new pediatric cases and a literature review-Reference-Cited by-同舟云学术

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A rare cause of facial nerve palsy in children: Hyperostosis corticalis generalisata (Van Buchem disease). Three new pediatric cases and a literature review

Published:2012-11 Issue:6 Volume:16 Page:740-743
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

van Egmond M.E.,Dikkers F.G.,Boot A.M.,van Lierop A.H.J.M.,Papapoulos S.E.,Brouwer O.F.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference9 articles.

1. Facial nerve palsy in the pediatric population;Shargorodsky;Clin Pediatr (Phila),2010

2. Glucocorticoids are not always deleterious for bone;van Lierop;J Bone Miner Res,2010

3. Case 150: Van Buchem disease (hyperostosis corticalis generalisata);Wengenroth;Radiology,2009

4. Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21;Van Hul;Am J Hum Genet,1998

5. Van Buchem disease: lifetime evolution of radioclinical features;Vanhoenacker;Skeletal Radiol,2003

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1. Papilledema: A review of etiology, pathophysiology, diagnosis, and management;Survey of Ophthalmology;2021-11

2. Van Buchem Disease: First Case Report from the Indian Subcontinent with an Early Presentation;Journal of Child Science;2021-01

3. Van Buchem disease;Medicine;2017-12

4. Maladie de Van Buchem;Revue du Rhumatisme;2017-10

5. Sclerostin deficiency in humans;Bone;2017-03

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