Revesz syndrome

Revesz syndrome is a rare variant of dyskeratosis congenita and is characterized by bilateral exudative retinopathy, alterations in the anterior ocular segment, intrauterine growth retardation, fine sparse hair, reticulate skin pigmentation, bone marrow failure, cerebral calcification, cerebellar hy...

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Bibliographic Details
Main Authors: Dayane Cristine Issaho, Ana Tereza Ramos Moreira, Lisandro Lima Ribeiro, Rommel Josué Zago, Christie Graf Ribeiro
Format: Article
Language:English
Published: Sociedade Brasileira de Oftalmologia 2015-04-01
Series:Revista Brasileira de Oftalmologia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0034-72802015000200110&lng=en&tlng=en