scholarly journals Deletion of chromosome 17 as a novel cytogenetic finding in chronic neutrophilic leukemia: A case report

2013 ◽  
Vol 5 (5) ◽  
pp. 1704-1706 ◽  
Author(s):  
YUANYUAN CHEN ◽  
SHUYE WANG ◽  
WEI WANG
2021 ◽  
Vol 13 (4) ◽  
pp. 116-122
Author(s):  
A. K. Polynnikova ◽  
O. E. Zinovyeva ◽  
O. A. Solokha ◽  
E. V. Misyuryaeva

Hereditary neuropathy with liability to pressure palsies (HNPP) is a rare hereditary disorder characterized by recurrent episodes of nerve compression. The first attack usually occurs in the second or third decade of life. In the majority of cases, HNPP is associated with a mutation at chromosome 17 p11.2-12 comprising the gene encoding peripheral myelin protein 22 (PMP22). Here we present a case report of a 43-year-old male with HNPP confirmed by DNA testing. The patient complained of recurrent episodes of bilateral foot extensor muscles weakness and/or hyperesthesia on the outer surface of the hands and forearms, which started after a prolonged posture maintaining and without evident precipitating factors. We also describe typical clinical, electrophysiological, and nerve ultrasound characteristics of the disease.


1986 ◽  
Vol 75 (6) ◽  
pp. 792-798
Author(s):  
Shinsuke KATO ◽  
Masanori SATO ◽  
Katsumi NAKAMURA

Cureus ◽  
2018 ◽  
Author(s):  
Bicky Thapa ◽  
Christopher Jamhour ◽  
Johnny Chahine ◽  
Heesun J Rogers ◽  
Hamed Daw

2015 ◽  
Vol 9 (5) ◽  
pp. 2208-2210 ◽  
Author(s):  
JINNING SHI ◽  
YING NI ◽  
JIANYONG LI ◽  
HAIRONG QIU ◽  
KOURONG MIAO

2004 ◽  
Vol 77 (4) ◽  
pp. 366-369 ◽  
Author(s):  
In Keun Choi ◽  
Byung-Soo Kim ◽  
Kyung-A Lee ◽  
Sookwon Ryu ◽  
Hee Yun Seo ◽  
...  

2013 ◽  
Vol 30 (S1) ◽  
pp. 77-79
Author(s):  
Sharada R. Rane ◽  
Maithili M. Kulkarni ◽  
Shaila C. Puranik

2014 ◽  
Vol 142 (suppl_1) ◽  
pp. A106-A106
Author(s):  
Christopher Wenzinger ◽  
Kalli Faulkner ◽  
Angie Duong ◽  
Alice Mims

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