extrinsic muscles
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2021 ◽  
Author(s):  
Juan L. Cobo ◽  
Sonsoles Junquera ◽  
José Martín-Cruces ◽  
Antonio Solé-Magdalena ◽  
Olivia García-Suárez ◽  
...  

The proprioception from the head is mainly mediated via the trigeminal nerve and originates from special sensitive receptors located within muscles called proprioceptors. Only muscles innervated by the trigeminal nerve, and rarely some muscles supplied by the facial nerve, contain typical proprioceptors, i.e. muscle spindles. In the other cephalic muscles (at the exception of the extrinsic muscles of the eye) the muscle spindles are replaced by sensory nerve formations (of different morphologies and in different densities) and isolated nerve fibers expressing mechanproteins (especially PIEZO2) related to proprioception. This chapter examines the cephalic proprioceptors corresponding to the territories of the trigeminal, facial, glossopharyngeal and hypoglossal nerves.


2021 ◽  
Vol 39 (2) ◽  
pp. 366-370
Author(s):  
Pamela Morales-Muñoz ◽  
Catalina Arriagada-Valdés ◽  
Jorge Sánchez-Oñate ◽  
Rodemil Medina-Puentes

2021 ◽  
Author(s):  
Wenjin Yan ◽  
Haijun Mao ◽  
Xingquan Xu ◽  
Liming Zheng ◽  
Pengjun Yu ◽  
...  

Abstract BackgroundCongenital cavus foot deformity (CFD) (congenital =present at birth) is a disease very disabling that could connected to the mobility, neurologic entities and the imbalance of synergistic intrinsic and extrinsic muscles of the patients, and the problem is even dynamic (often progressive). Here, we report the clinical and radiographic manifestations of one Chinese Han congenital CFD family and 23 congenital CFD patients. In the congenital CFD family, the proband’s mother and brother are also CFD patients. ResultsWe performed whole-exome sequencing for three patients and two healthy people in this family, and sequenced the Frizzled Class Receptor 4 (FZD4) for the other. One novel FZD4 mutation (exon2 c.1589G>A; p.G530E, NM_012193) was identified. Then mutations in FZD4 gene were further examined in 23 congenital CFD patients, and also find FZD4 mutation (FZD4:NM_012193:exon1:c.205C>T:p.H69Y) in one congenital CFD patient. ConclusionsOur study suggested that the congenital cavus foot deformity might be associated with the identified mutations in FZD4.


2020 ◽  
Vol 17 (4) ◽  
pp. 046033
Author(s):  
Simone Tanzarella ◽  
Silvia Muceli ◽  
Alessandro Del Vecchio ◽  
Andrea Casolo ◽  
Dario Farina

2019 ◽  
Author(s):  
Craig Hacking ◽  
Daniel Bell

2018 ◽  
Vol 30 (3) ◽  
pp. 355-360
Author(s):  
Masahiro Mitsukane ◽  
Noboru Sekiya ◽  
Arinori Kamono ◽  
Tohru Nakabo

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