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Genet Couns ; 26(1): 35-9, 2015.
Article in English | MEDLINE | ID: mdl-26043505

ABSTRACT

Joubert Syndrome is a rare autosomal recessive disorder characterized by absence or underdevelopment of the cerebellar vermis. Various ocular and oculomotor findings are frequently seen in cases with Joubert Syndrome. However, only three adolescent patients with Joubert Syndrome were diagnosed with optic disc drusen. Here we present an infant case of Joubert Syndrome referred with papilledema and diagnosed with optic disc drusen.


Subject(s)
Cerebellar Diseases/complications , Eye Abnormalities/complications , Kidney Diseases, Cystic/complications , Optic Disk Drusen/etiology , Retina/abnormalities , Abnormalities, Multiple , Cerebellum/abnormalities , Female , Humans , Infant , Optic Disk Drusen/diagnosis , Papilledema/diagnosis
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