Results 111 to 120 of about 36,996 (247)
Proptosis in a family with the p16 Leue-to-Prol mutation in the PMP22 gene (CMT 1E) [PDF]
Univ Fed Paulista UNIFESP, Dept Neurol, São Paulo, BrazilUniv São Paulo, Fac Med Ribeirao Preto, Dept Neurociencias & Ciencias Comportamento, Ribeirao Preto, SP, BrazilUniv Fed Paulista UNIFESP, Dept Neurol, São Paulo, BrazilWeb of ...
Calia, Leandro +4 more
core +2 more sources
Orbital Oculomotor Nerve Schwannoma Extending to the Cavernous Sinus: A Rare Cause of Proptosis
PURPOSE To report a case of orbital oculomotor nerve schwannoma extending to the cavernous sinus through the superior orbital fissure presenting with proptosis, but without any neurological sign.
Hina Kauser +3 more
semanticscholar +1 more source
Malignant Melanoma of Nose and Paranasal Sinuses: 2 Case Reports [PDF]
Malignant melanoma is one of the rare and highly aggressive diseases of the sinonasal cavity. High index of suspicion is required for diagnosis as the patient usually presents with non specific signs and symptoms.
Bhagat, S +4 more
core +1 more source
BackgroundThe purpose of this retrospective follow-up study is to evaluate the prevalence of patients with thyroid eye disease presenting with apparent unilateral proptosis and determine the occurrence of exophthalmos in contralateral non-proptotic eye ...
D. Strianese +15 more
semanticscholar +1 more source
Effects of Ethmoid Surgery on Proptosis and Vision
Objective:To evaluate the role of external ethmoidectomy in improvement of proptosis and vision due to ethmoid disease. Materials and Methods: This interventional study was conducted in the department of Otorhipolaryngology and Head and Neck Surgery ...
Masood Akhtar +4 more
doaj
Bilateral proptosis caused by orbital myositis. A case report
Proptosis, unilateral or bilateral, is a frequent indication for medical evaluation and orbital computed tomography. The most common cause of proptosis in adults and children is inflammatory disorders. Orbital myositis is a subgroup of the orbital
K Aydin +5 more
doaj
Multiple café au lait macules are one of the cornerstones in diagnosing neurofibromatosis Type 1 (NF 1). NF 1 is often a multisystem neurocutaneous disorder, plexiform NF being one of the most important variants of this phacomatosis. Here, a rare case of
Aniruddha Ghosh +3 more
doaj +1 more source
Enophthalmos caused by an orbital venous malformation [PDF]
Orbital vascular malformations usually present with proptosis. We report a case where a patient with an orbital venous malformation presented with enophthalmos.
Chung, CF, Lai, JSM
core
Tratamiento de la orbitopatía de Graves [PDF]
Nuestro objetivo es realizar un resumen de la patología orbitaria en la enfermedad tiroidea, sus herramientas diagnósticas y las medidas terapéuticas actualizadas, basado en la evidencia científica de la bibliografía específica.
Bustos, Isaías Eduardo
core +1 more source
AN ETIOLOGICAL ANALYSIS OF CHILDHOOD PROPTOSIS
AIMS: To analyse the various causes for proptosis in Children. SETTINGS AND DESIGN: Prospective analytical study. METHODS AND MATERIAL: A prospective analysis of 50 cases of proptosis in children less than 15 years.
M. Loganathan, M. Radhakrishnan
semanticscholar +1 more source

