Literature DB >> 4015878

Congenital ectropion uveae and glaucoma.

R Hertzberg.   

Abstract

Congenital ectropion uveae is a rare condition which may be present in one or both eyes. If the patient is followed glaucoma will always be found to be present. Associated features which have been described are ptosis, Rieger's anomaly, Prader Willi syndrome, facial hemiatrophy and neurofibromatosis. This paper describes a patient followed for 18 years who had bilateral congenital ectropion uveae, bilateral ptosis, asthma and late onset of a dental defect.

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Year:  1985        PMID: 4015878     DOI: 10.1111/j.1442-9071.1985.tb00398.x

Source DB:  PubMed          Journal:  Aust N Z J Ophthalmol        ISSN: 0814-9763


  3 in total

1.  Primary iris pigment epithelial hyperplasia and glaucoma.

Authors:  A Bansal; J Luck
Journal:  Br J Ophthalmol       Date:  2002-03       Impact factor: 4.638

2.  CO2 Laser-Assisted Sclerectomy vs. Microcatheter-Assisted Trabeculotomy in the Management of a Bilateral Congenital Ectropion Uveae With Glaucoma: A Case Report and Literature Review.

Authors:  Min Chen; Yuhang Li; Bo Cheng; Qi Zhang; Xin Liu; Kaijun Wang
Journal:  Front Med (Lausanne)       Date:  2022-05-19

3.  A young Botswana patient with congenital iris ectropion uvea.

Authors:  Jemal Zeberga Shifa; Othokawa Nkomazana; Negussie Alula Bekele; Mamo Woldu Kassa
Journal:  Pan Afr Med J       Date:  2016-09-29
  3 in total

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