نتایج جستجو برای: horner syndrome

تعداد نتایج: 622322  

Journal: :Case Reports in Endocrinology 2017

2017
Bouthouri Abir Mansour Malek

Wegener’s granulomatosis(WG) is a systemic necrotising granulomatous vasculitis. The central nervous system(CNS) manifestations are rare. A 49-year-old man, presented with sudden onset of left-sided weakness. Physical examination revealed pyramidal syndrome with left-sided hemiparesis, right kinetic cerebellar syndrome and right Horner syndrome. Examination of the cardiovascular system was norm...

Journal: :Ağrı - The Journal of The Turkish Society of Algology 2016

Journal: :archives of pediatric infectious diseases 0
olivier gilliaux department of pediatrics, hôpital civil marie curie, charleroi, belgium valerie ghilain department of pediatrics, cliniques universitaires saint-luc, université catholique de louvain (ucl), brussels, belgium dimitri van der linden department of pediatrics, cliniques universitaires saint-luc, université catholique de louvain (ucl), brussels, belgium jean philippe stalens department of pediatrics centre, centre hospitalier wallonie picarde, tournai, belgium catherine heijmans department of pediatrics, centre hospitalier de jolimont, haine-saint-paul, belgium jacques louis department of pediatrics, grand hôpital de charleroi, charleroi, belgium

conclusions this paper highlighted the need to exclude csd in children with unexplained symptoms such as prolonged fever, hepatosplenic lesion and osteomyelitis. case presentation we reported a series of seven children with unusual symptoms of csd. in particular, we described the case of a child with ptosis, miosis and enophtalmy, suggesting horner syndrome, associated with cervical lymphadenit...

Journal: :Revista Mexicana de Oftalmología (English Edition) 2019

2017
Jeremias Motte Ilonka Kreitschmann-Andermahr Anna Lena Fisse Christian Börnke Christoph Schroeder Kalliopi Pitarokoili Oliver Müller Carsten Lukas Johannes van de Nes Rolf Buslei Ralf Gold Ilya Ayzenberg

OBJECTIVE To report a rare case of incipient granulomatous hypophysitis presenting by atypical trigemino-autonomic cephalalgia (TAC) and Horner syndrome. METHODS The patient was investigated with repeated brain MRI, CSF examination, thoracic CT, Doppler and duplex ultrasound of the cerebral arteries, and extensive serologic screening for endocrine and autoimmune markers. Written informed cons...

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