Repository logo
 
Loading...
Thumbnail Image
Publication

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

Use this identifier to reference this record.
Name:Description:Size:Format: 
Case Rep Pediatr 2012_ID382657.pdf42.51 KBAdobe PDF Download

Advisor(s)

Abstract(s)

Hereditary 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.

Description

Keywords

Neuropatia Hereditária Motora e Sensorial Mão Criança HDE MFR HDE NEU PED

Pedagogical Context

Citation

Case Rep Pediatr.2012:Article ID 382657

Research Projects

Organizational Units

Journal Issue

Publisher

Hindawi Publishing Corporation

CC License