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Case Report

Cataract surgery in Knobloch syndrome: a case report

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Pages 735-737 | Published online: 02 Jun 2011

References

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  • Passos-BuenoMRSuzukiOTArmelin-CorreaLMMutations in collagen 18A1 and their relevance to the human phenotypeAn Acad Bras Cienc200678112313116532212
  • Passos-BuenoMRMarieSKMonteiroMKnobloch syndrome in a large Brazilian consanguinous family: Confirmation of autosomal recessive inheritanceAm J Med Genet19945221701737802003
  • SertieALQuimbyMMoreiraESA gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3Hum Mol Genet1996568438478776601
  • DuhEJYaoYGDagliMGoldbergMFPersistence of fetal vasculature in a patient with Knobloch syndrome: Potential role for endostatin in fetal vascular remodeling of the eyeOphthalmology2004111101885188815465551
  • SertieALSossiVCamargoAAZatzMBraheCPassos-BuenoMRCollagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)Hum Mol Genet20009132051205810942434
  • MahajanVBOlneyAHGarrettPCharyADraganELernerGCollagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemiaAm J Med Genet Part A2010152A112875287920799329
  • TartarellaMBVerçosaITécnicas cirúrgicas da catarata na criança [Surgical techniques for cataract in children]VerçosaITartarellaMBCatarata na Criança [Cataract in Children].Fortaleza, BrazilEditora Celigráfica2008