Repository logo
 
Publication

Hereditary Neuropathy with Liability to Pressure Palsy Presenting with Hand Drop in a Young Child

dc.contributor.authorSobreira, I
dc.contributor.authorSousa, C
dc.contributor.authorRaposo, A
dc.contributor.authorSoares, MR
dc.contributor.authorSoudo, AP
dc.contributor.authorDias, AI
dc.date.accessioned2014-03-25T10:54:53Z
dc.date.available2014-03-25T10:54:53Z
dc.date.issued2012
dc.description.abstractHereditary neuropathy with liability to pressure palsy (HNPP) results from the deletion of the PMP22 gene in chromosome 17p11.2. Clinically, it presents with painless pressure palsies, typically in the 2nd and 3rd decades of life, being a rare entity in childhood. We present the case study of a six-year-old male child who presented with left hand drop that he kept for over four weeks. Electrophysiological studies suggested HNPP and genetic studies confirmed it. With this paper, we pretend to create awareness to this entity as a diagnosis to be considered in a child with painless monoparesis and to emphasize the importance of electrophysiological studies in the diagnosis.por
dc.identifier.citationCase Rep Pediatr.2012:Article ID 382657por
dc.identifier.urihttp://hdl.handle.net/10400.17/1748
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherHindawi Publishing Corporationpor
dc.subjectNeuropatia Hereditária Motora e Sensorialpor
dc.subjectMãopor
dc.subjectCriançapor
dc.subjectHDE MFRpor
dc.subjectHDE NEU PEDpor
dc.titleHereditary Neuropathy with Liability to Pressure Palsy Presenting with Hand Drop in a Young Childpor
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Case Rep Pediatr 2012_ID382657.pdf
Size:
42.51 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: