Vagus nerve pressure palsy in hereditary neuropathy with liability to pressure palsies confirmed by neurosonography

2021 ◽  
Vol 132 (4) ◽  
pp. 975-976
Author(s):  
Patrick Steinwand ◽  
Alexander Grimm ◽  
Georg L.F. Potthast ◽  
Ulf Ziemann ◽  
Markus Krumbholz
2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Inês Sobreira ◽  
Cátia Sousa ◽  
Ana Raposo ◽  
M. Rita Soares ◽  
Ana Soudo ◽  
...  

Hereditary neuropathy with liability to pressure palsy (HNPP) results from the deletion of thePMP22gene 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.


2016 ◽  
Vol 74 (2) ◽  
pp. 99-105 ◽  
Author(s):  
Aline Pinheiro Martins de Oliveira ◽  
Raquel Campos Pereira ◽  
Patrícia Toscano Onofre ◽  
Vanessa Daccach Marques ◽  
Gilberto Brown de Andrade ◽  
...  

ABSTRACT The hereditary neuropathy with liability to pressure palsies (HNPP) is an autossomal dominant disorder manifesting recurrent mononeuropathies. Objective Evaluate its clinical and nerve conduction studies (NCS) characteristics, searching for diagnostic particularities. Method We reviewed the neurological manifestations of 39 and the NCS of 33 patients. Results Family history was absent in 16/39 (41%). The onset complaints were weakness in 24, pain in 6, sensory deficit in 5 and paresthesias in 4. Pain was seen in 3 other patients. The following neuropathy patterns were found: multiple mononeuropathy (26), mononeuropathy (7), chronic sensorimotor polyneuropathy (4), chronic sensory polyneuropathy (1) and unilateral brachial plexopathy (1). NCS showed a sensorimotor neuropathy with focal conduction slowing in 31, two had mononeuropathy and another brachial plexopathy. Conclusion HNPP presentation is variable and may include pain. The most frequent pattern is of an asymmetrical sensory and motor neuropathy with focal slowing at specific topographies on NCS.


2003 ◽  
Vol 29 (2) ◽  
pp. 205-210 ◽  
Author(s):  
Jun Li ◽  
Karen Krajewski ◽  
Richard A. Lewis ◽  
Michael E. Shy

2007 ◽  
Vol 3 (2) ◽  
pp. 208-212 ◽  
Author(s):  
Marc J. Grossman ◽  
Joseph Feinberg ◽  
Edward F. DiCarlo ◽  
Sherri B. Birchansky ◽  
Scott W. Wolfe

2017 ◽  
Vol 7 (9) ◽  
pp. e00783 ◽  
Author(s):  
Minori Kodaira ◽  
Satoshi Kodama ◽  
Yui Kamijo ◽  
Tomoki Kaneko ◽  
Yoshiki Sekijima

2017 ◽  
Vol 43 (1) ◽  
Author(s):  
Carlo Fusco ◽  
Carlotta Spagnoli ◽  
Grazia Gabriella Salerno ◽  
Elena Pavlidis ◽  
Daniele Frattini ◽  
...  

2014 ◽  
Vol 37 (2) ◽  
pp. 106-111 ◽  
Author(s):  
Ayse O. Bayrak ◽  
Ilkay Koray Bayrak ◽  
Esra Battaloglu ◽  
Burcak Ozes ◽  
Onur Yildiz ◽  
...  

2015 ◽  
Vol 29 (11) ◽  
pp. 83 ◽  
Author(s):  
Hyoung Won Choi ◽  
Nancy L. Kuntz

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