Vision in Ehlers-Danlos syndrome. Role of orthoptics
نویسندگان
چکیده
Ehlers-Danlos disease, usually called syndrome, is an inherited connective tissue disorder that spares the central nervous system except in its component. It manifested by a set of symptoms and clinical signs which are expression tissue’s frailty. Visual manifestations explained fragility proprioception disturbance increased muscle dysfunctions: cornea’s fragility, photophobia, diplopia, blepharospasms, eyelids’ retractions, myopia, astigmatism. The orthoptist’s role to help prescription prism correction rather than rehabilitation, ineffective. In combination, global effect treatments, particular for dystonia, dysautonomia… essential this frequent poorly described therefore very seldom diagnosed. transmitted all children affected person. objective work contribute diagnosis disease more often frequently families. orthoptist's important because diplopia has functional consequences. Pine-hole glasses may give some relief filtering out light dazzles these patients significantly.
منابع مشابه
[Ehlers-Danlos syndrome].
We have described a patient with type 4 Ehlers-Danlos syndrome who died of a ruptured pulmonary artery. Of the six subtypes of Ehlers-Danlos syndrome, which can usually be clinically differentiated, only types 1 and 4 appear to be associated with a substantial risk of arterial rupture.
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Twenty patients with the Ehlers-Danlos syndrome, (10 type I, six type II, and four type IV) were studied to assess the frequency of respiratory abnormalities in this condition. Five patients (25%) had had at least one episode of haemoptysis, but none had any defect of coagulation. There was a high frequency of recurrent sinusitis, notably in those with the type I syndrome. Two patients had bull...
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The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of skin and hypermobility of joints to differing extents. The skin is easily injured and wound healing is delayed. The majority of EDS patients belong to EDS-types I-III. The pathogenesis in these cases is not known, although recent data suggest a role...
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PURPOSE Ehlers-Danlos syndrome (EDS) is a complex hereditary connective tissue disorder infrequently reported in association with epilepsy. Seven patients with ages ranging from 28 to 70 years with EDS and epilepsy are described. METHODS Case review of clinical and diagnostic data. RESULTS Two patients had occipital horn syndrome (EDS type IX) and partial seizures of probable supplementary ...
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ژورنال
عنوان ژورنال: Journal of clinical research and ophthalmology
سال: 2022
ISSN: ['2455-1414']
DOI: https://doi.org/10.17352/2455-1414.000098