Assessment and Grading of Synkinesisand Facial Palsy

2022 ◽  
pp. 51-58
Author(s):  
Helen Hartley ◽  
Wendy Blumenow ◽  
Rebecca Williams ◽  
Adel Fattah
Keyword(s):  
Facial Palsy

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

2013 ◽  
Vol 44 (02) ◽  
Author(s):  
J Brunner ◽  
RW Reinhard ◽  
LB Zimmerhackl
Keyword(s):  
Facial Palsy ◽  
Lyme Neuroborreliosis

Incidence and Risk Factors of Delayed Facial Palsy after Vestibular Schwannoma Resection

2015 ◽  
Vol 76 (S 01) ◽  
Author(s):  
Lucas Carlstrom ◽  
William Copeland ◽  
Brian Neff ◽  
Colin Driscoll ◽  
Michael Link
Keyword(s):  
Risk Factors ◽  
Vestibular Schwannoma ◽  
Facial Palsy

Management of Traumatic Facial Palsy

Skull Base ◽  
2008 ◽  
Vol 18 (S 01) ◽  
Author(s):  
Tony Cheesman
Keyword(s):  
Facial Palsy

Neurological manifestation in severe hypothyroidism in pregnancy

2020 ◽  
Vol 13 (12) ◽  
pp. e238069
Author(s):  
Aparna Sharma ◽  
Nilofar Noor ◽  
Vatsla Dadhwal
Keyword(s):  
Peripheral Neuropathy ◽  
Facial Palsy ◽  
Caesarean Delivery ◽  
Thyroid Stimulating Hormone ◽  
Neurological Manifestations ◽  
Second Trimester ◽  
Pituitary Hyperplasia ◽  
Very High ◽  
In Pregnancy

Neurological manifestations of hypothyroidism include peripheral neuropathy and pituitary hyperplasia. However, these associations are rarely encountered during pregnancy. We report a case of a known hypothyroid with very high thyroid stimulating hormone (TSH) values (512 μIU/mL) in the second trimester. At 24 weeks she developed facial palsy and pituitary hyperplasia which responded to a combination of steroids and thyroxine. She had caesarean delivery at 35 weeks and 3 days gestation in view of pre-eclampsia with severe features and was discharged on oral antihypertensives and thyroxine. On follow-up at 5 months, TSH normalised and pituitary hyperplasia showed a greater than 50% reduction in size. To our knowledge, this is the first reported case of facial palsy and pituitary hyperplasia associated with hypothyroidism during pregnancy.

scholarly journals Congenital unilateral facial palsy revealing a facial nerve agenesis: a case report and review of the literature

2019 ◽  
Vol 5 (1) ◽  
pp. 20180029
Author(s):  
Yaotse Elikplim Nordjoe ◽  
Ouidad Azdad ◽  
Mohamed Lahkim ◽  
Laila Jroundi ◽  
Fatima Zahrae Laamrani
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Temporal Bone ◽  
Facial Paralysis ◽  
Facial Palsy ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Moebius Syndrome ◽  
Temporal Bone Ct

Facial nerve aplasia is an extremely rare condition that is usually syndromic, namely, in Moebius syndrome. The occurrence of isolated agenesis of facial nerve is even rarer, with only few cases reported in the literature. We report a case of congenital facial paralysis due to facial nerve aplasia diagnosed on MRI, while no noticeable abnormality was detected on the temporal bone CT.

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