CONGENITAL HYPOPLASIA OF THE DEPRESSOR ANGULI ORIS MUSCLE IN THE DIFFERENTIAL DIAGNOSIS OF FACIAL PARALYSIS

1983 ◽  
Vol 93 (9) ◽  
pp. 1168???1170 ◽  
Author(s):  
STEVEN J. MILLEN ◽  
J. K. BARUAH
Trials ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Binyan Yu ◽  
Lihua Xuan ◽  
Yutong Jin ◽  
Shan Chen ◽  
Shan Liu ◽  
...  

Abstract Background Facial expression muscles atrophy is one kind of sequelae after peripheral facial paralysis. It causes critical problems in facial appearance of patient as well as social and psychological problems. This study aims to evaluate the efficacy and safety of Thread-embedding acupuncture (TEA) for the management of facial expression muscles atrophy after peripheral facial paralysis. Methods This is a patient-assessor blinded, randomized, sham-controlled trial. A total of fifty-six eligible patients will be randomly divided into TEA (n=28) and sham TEA (STEA) (n=28) groups. Both groups will receive TEA or STEA treatment at the frontal muscle and the depressor anguli oris muscle, at one predefined points once a week for eight weeks. Additionally, both groups will receive traditional acupuncture treatment at ten acupoints (GB20, LI4, LR3, GB12, ST7, SI18, LI20, BL2, SJ23, ST4) twice a week for eight weeks as a concurrent treatment. B-mode ultrasonography will be used to assess the changes in facial expression muscle thickness ratio of the affected/healthy side at baseline and at 10 weeks after screening, as the primary outcome. House-Brackmann Grade and lip mobility score will be measured and analyzed at baseline and 4, 8, 10, and 12 weeks after screening, as secondary outcomes. Discussion The study will compare TEA with sham TEA to explore the feasibility for TEA in improving facial expression muscles atrophy after peripheral facial paralysis. Trial registration Chinese Clinical Trial Registry, ChiCTR1900027170. Registered on 3 November 2019, http://www.chictr.org.cn/edit.aspx?pid=45173&htm=4


1981 ◽  
Vol 89 (5) ◽  
pp. 841-848 ◽  
Author(s):  
Mark May ◽  
Thomas J. Fria ◽  
Frank Blumenthal ◽  
Hugh Curtin

The differential diagnosis in 170 patients between birth and 18 years of age is reviewed. There are a number of obvious physical findings and historical features that allow one to make a diagnosis rather quickly. Pain, vesicles, a red pinna, vertigo, and sensorineural hearing loss suggest herpes zoster oticus. Slow progression beyond three weeks, recurrent facial paralysis involving the same side, facial twitching, weakness, or no return of function after six months indicate a neoplasm. Bilateral simultaneous facial paralysis indicates a cause other than Bell's palsy, such as Guillain-Barré syndrome, pseudobulbar palsy, sarcoidosis, and leukemia. Recurrent facial paralysis associated with a fissured tongue, facial edema, and a positive family history should suggest Melkersson-Rosenthal syndrome.


PEDIATRICS ◽  
1972 ◽  
Vol 50 (1) ◽  
pp. 171-171
Author(s):  
Saul D. Roskes

The review paper by Drs. Manning and Adour on facial paralysis in childhood was illuminating in terms of differential diagnosis. However, one very important consideration in the assessment of children who present with peripheral facial paralysis is the possibility that it may be the initial manifestation of severe hypertension in children. It is presumed that the paralysis is due to hemorrhage within the facial canal. Because hypertension in childhood very frequently has an etiology which is surgically or medically remediable the index of suspicion for its presence must be maintained at a high level.


2016 ◽  
Vol 22 (4) ◽  
pp. 196-198 ◽  
Author(s):  
Nihan Hande Akçakaya ◽  
Meltem Hale Alpsan Gökmen ◽  
Yeşim Gülşen Parman ◽  
Feza Deymeer ◽  
Piraye Oflazer

1988 ◽  
Vol 98 (1) ◽  
pp. 53-59 ◽  
Author(s):  
Carl Snyderman ◽  
Mark May ◽  
Michael A. Berman ◽  
Hugh D. Curtin

Traumatic neuromas (TN) are benign proliferations of neural tissue that may occur without disruption of the facial nerve. The clinical presentation, as well as the radiographic appearance, may suggest neoplastic involvement of the facial nerve. Histologically, they may closely resemble neurilemomas (Schwannomas) or neurofibromas. Three cases of TN of the facial nerve associated with facial paralysis are presented here. Unlike previously reported cases, these tumors were not associated with chronic inflammatory middle ear disease. TN must be considered in the differential diagnosis and treatment of facial paralysis.


1986 ◽  
Vol 100 (10) ◽  
pp. 1187-1193
Author(s):  
W. H. Moesker ◽  
R. A. Tange

SummaryWe present two patients, mother and daughter, with a skeletal disorder of the skull, hearing loss and in one of them recurrent facial paralysis. In one patient middle ear exploration was performed. The malleus and incus were found to be fixed in the epitympanum.The differential diagnosis is discussed. We reviewed all known hereditary conditions with hearing loss and musculoskeletal disease but we could not accept any of these diagnoses for our patients.


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