2006
DOI: 10.4321/s0365-66912006000600004
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Distrofia macular corneal: características clínicas, histopatológicas y ultraestructurales

Abstract: Females were more affected than males and the mean age at the time of diagnosis was older than that reported previously, however the clinical, histopathological and ultrastructural features were similar to those of previous reports. As described in other cases in the literature, in some instances a disorder is found in CHST6 gene as a basis for this condition.

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Cited by 9 publications
(2 citation statements)
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“…It is characterized by being an autosomal recessive disorder in the CHST6 gene, presenting an alteration in keratan sulfate metabolism. Histologically it is characterized by extracellular deposits of glycosaminoglycans between stromal lamellae as well as in the cytoplasm of endothelial cells [4].…”
Section: Discussionmentioning
confidence: 99%
“…It is characterized by being an autosomal recessive disorder in the CHST6 gene, presenting an alteration in keratan sulfate metabolism. Histologically it is characterized by extracellular deposits of glycosaminoglycans between stromal lamellae as well as in the cytoplasm of endothelial cells [4].…”
Section: Discussionmentioning
confidence: 99%
“…Se trata de una alteración en la síntesis del queratán-sulfato con manifestaciones sistémicas. Es de Calidad óptica ocular en ojos sometidos a cirugía refractiva y afecciones patológicas -40 herencia autosómica recesiva que la hace menos común pero más severa: bilateral, simétrica, difusa y precoz (Gulias-Canizo, Castaneda-Diez et al 2006).…”
Section: Distrofia Macularunclassified