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1.
BMC Ophthalmol ; 17(1): 200, 2017 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-29110702

RESUMO

BACKGROUND: Ocular contusion can produce severe lesions, which if not treated appropriately and promptly, can lead to visual impairment. Ocular contusion in childhood may not be reported by children. CASE PRESENTATION: A 27 year old female presented with a partially absorbed cataractous lens that was dislocated into the anterior chamber of her left eye. There was mild anterior chamber reaction. She reported no history of ocular trauma; but associated findings and further investigations were in favour of a post-traumatic aetiology. CONCLUSION: All ocular injuries require a detailed ophthalmological examination to assess vision and the extent of lesions.


Assuntos
Câmara Anterior/patologia , Catarata/patologia , Traumatismos Oculares/complicações , Subluxação do Cristalino/patologia , Adulto , Feminino , Humanos , Cristalino/patologia
2.
Pan Afr Med J ; 23: 99, 2016.
Artigo em Francês | MEDLINE | ID: mdl-27231508

RESUMO

Usher syndrome is defined by the association of a progressive or non-progressive congenital sensorineural hearing loss with variable severity and a gradually blinding pigmentary retinopathy. Von Recklinghausen neurofibromatosis or Neurofibromatosis type 1 is the major clinically form of neurofibromatosis which occurs in approximately 90% of cases. Both types of disease are genetic in origin with very low prevalence. The probability of co-occurrence of these diseases in a single individual is exceptional. Inbreeding, as well as all genetic diseases, increases quite significantly the probability of their occurrence. Consanguineous marriages are still widespread in Maghreb and in some regions of the western African. This observation reports an exceptional case of this association in a 40-year-old man of Mauritanian origin born from a consanguineous union.


Assuntos
Consanguinidade , Neurofibromatose 1/fisiopatologia , Síndromes de Usher/fisiopatologia , Adulto , África do Norte , Humanos , Masculino , Neurofibromatose 1/genética , Síndromes de Usher/genética
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