scholarly journals Parry-Romberg syndrome in Kuwait. Neurological manifestations in 2 children

2019 ◽  
Vol 40 (7) ◽  
pp. 721-726 ◽  
Author(s):  
Mohamed Zakkiriah ◽  
Maryam Al Khalaf ◽  
Muna Al Mutairi ◽  
Sarah Al Enezi
Medicine ◽  
2015 ◽  
Vol 94 (28) ◽  
pp. e1147 ◽  
Author(s):  
Justine Vix ◽  
Stéphane Mathis ◽  
Mathieu Lacoste ◽  
Rémy Guillevin ◽  
Jean-Philippe Neau

2012 ◽  
Vol 79 (4) ◽  
pp. 419-421 ◽  
Author(s):  
João Madruga Dias ◽  
Maria Manuela Costa ◽  
José Alberto Pereira da Silva ◽  
Mário Viana de Queiroz

Author(s):  
Tasleem Arif ◽  
Rafiya Fatima ◽  
Marwa Sami

2017 ◽  
Vol 79 (5) ◽  
pp. 473-477
Author(s):  
Keiko MATSUMOTO ◽  
Ken SHIRAISHI ◽  
Mikiko TOHYAMA ◽  
Kensuke SENZAKI ◽  
Koji SAYAMA

2020 ◽  
Vol 3 (1) ◽  
pp. 6-8
Author(s):  
Zufar ADAMBAEV ◽  
◽  
Ibodulla KILICHEV ◽  
Tuygunoy XODJANOVA

A complex therapy of patients with degenerative-dystrophic diseases of the spine with herniated intervertebral discs with neurological manifestations was carried out with the addition of phonophoresis Kariflex gel followed by segmental massage with Kariflex cream. The comparative evaluation of the method was carried out in 89 patients. Comparative analysis revealed the reliable efficiency of the method used. Against the background of the proposed therapy, there was a significant decrease in pain and muscle-tonic syndromes, an increase in the range of motion in the spine


2018 ◽  
Vol 0 (2) ◽  
pp. 18-24
Author(s):  
O. O. Kopchak ◽  
T. A. Odintsova ◽  
N. Yu. Bachynska

2020 ◽  
Author(s):  
Giovanna Travi ◽  
Roberto Rossotti ◽  
Marco Merli ◽  
Federico D'Amico ◽  
Stefania Chiappetta ◽  
...  

2020 ◽  
Vol 13 (12) ◽  
pp. e238069
Author(s):  
Aparna Sharma ◽  
Nilofar Noor ◽  
Vatsla Dadhwal

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.


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