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Published in 2023 at "Medicine"
DOI: 10.1097/md.0000000000032869
Abstract: Background: In January 2021, we found one case of Axenfeld–Rieger syndrome combined with pigment dispersion syndrome (PDS), and this patient additionally manifested a symptom of ectropion uveae. The co-existence of both 2 syndromes is very…
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Keywords:
axenfeld rieger;
ectropion uveae;
rieger syndrome;
dispersion ... See more keywords
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Published in 2019 at "European Journal of Ophthalmology"
DOI: 10.1177/1120672119860379
Abstract: We report the case of congenital ectropion uveae in a 10-year-old boy with intractable unilateral glaucoma but no systemic association. Glaucoma in congenital ectropion uveae is often poorly responsive to medial therapy and requires surgical…
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Keywords:
uveae ceu;
ectropion uveae;
congenital ectropion;
refractory glaucoma ... See more keywords
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1
Published in 2022 at "European Journal of Ophthalmology"
DOI: 10.1177/11206721221111595
Abstract: Purpose To evaluate the long-term outcomes of glaucoma management in patients with congenital ectropion uveae (CEU) over a period of three decades at a single large referral tertiary eye care center. Methods Retrospective chart review…
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Keywords:
ectropion uveae;
glaucoma management;
glaucoma;
iop ... See more keywords
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1
Published in 2023 at "European journal of ophthalmology"
DOI: 10.1177/11206721231156501
Abstract: A 18-year-old woman with unilateral glaucoma secondary to congenital ectropion uveae (CEU) in the right eye, without other systemic and ocular associations. Intraocular pressure (IOP) was uncontrolled under topical therapy. The visual field (VF) was…
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Keywords:
ectropion uveae;
mmhg;
therapy;
case ... See more keywords
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Published in 2022 at "Romanian Journal of Ophthalmology"
DOI: 10.22336/rjo.2022.25
Abstract: Aim: To report the cases of five children with unilateral advanced glaucoma in isolated congenital ectropion uveae (CEU) with ipsilateral ptosis and myopia. Methods: This is an ambispective observational case series. After diagnosing one patient…
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Keywords:
ectropion uveae;
ectropion;
glaucoma;
five children ... See more keywords
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1
Published in 2021 at "Annali di igiene : medicina preventiva e di comunita"
DOI: 10.7417/ct.2021.2314
Abstract: Abstract Neurofibromatosis type 1 (NF1) is a rare genetic disorder with an autosomal dominant transmission and an estimated incidence of 1:2500-3500 live birth. Penetrance is virtually 100%, but the expression is highly variable and almost…
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Keywords:
nf1;
neurofibromatosis type;
ectropion uveae;
uveae neurofibromatosis ... See more keywords