Evidence map›Paper›PMID 37946776›Full record

ArticleWorld journal of clinical cases2023

Axenfeld-Reiger syndrome: A search for the missing links.

Arvind Kumar Morya, Prasanna Venkatesh Ramesh, Sony Sinha, Prateek Nishant, Nazia Nain, Ravi Naik Ramavath, Chetana Gone, Ripunjay Prasad

Abstract read
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Article in World journal of clinical cases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Arvind Kumar MoryaDepartment of Ophthalmology, All India Institute of Medical Sciences, Bibi Nagar, Hyderabad 508126, Telangana, India. bulbul.morya@gmail.com.
Prasanna Venkatesh RameshGlaucoma Medical Officer, Mahathma Eye Hospital Private Limited, Thennur, Trichy 620017, Tamil Nadu, India.
Sony SinhaDepartment of Ophthalmology-Vitreo-Retina and Oculoplasty, All India Institute of Medical Sciences, Patna, Patna 801507, Bihar, India.
Prateek NishantDepartment of Ophthalmology, All India Institute of Medical Sciences, Patna, Patna 801507, Bihar, India.
Nazia NainDepartment of Ophthalmology, All India Institute of Medical Sciences, Bibi Nagar, Hyderabad 508126, Telangana, India.
Ravi Naik RamavathDepartment of Ophthalmology, All India Institute of Medical Sciences, Bibi Nagar, Hyderabad 508126, Telangana, India.
Chetana GoneDepartment of Ophthalmology, All India Institute of Medical Sciences, Bibi Nagar, Hyderabad 508126, Telangana, India.
Ripunjay PrasadDepartment of Ophthalmology, RP Eye Institute, Delhi 110001, Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAxenfeld-Rieger syndrome (ARS) is a rare cause of congenital glaucoma and may result in loss of vision. ARS is mostly autosomal dominant in nature characterized by developmental abnormalities in the angle of anterior chamber and iris of the eye, also associated with structural abnormalities in the body.

aimTo study and observe the demographics and clinical findings in a very rare ocular disease known as ARS.

methodsCase records of symptomatic patients attending Ophthalmology outpatient department and diagnosed to have ocular hypertension or glaucoma in 3 years from March 2017 to March 2020 were evaluated to search for cases diagnosed with ARS. Records of all patients diagnosed with ARS were then analysed for demographic and clinical characterization as well as management and success of therapy.

resultsEight out of ten patients with positive clinical signs were symptomatic and had glaucoma. One of these patients had limbal stem cell deficiency and another had vernal keratoconjunctivitis.

conclusionClinical characterization of ARS is important for making a definitive diagnosis and determining prognosis.

Indexed as

Axenfeld-Reiger SyndromeGlaucomaLimbal stem cell deficiencyVernal keratoconjuctivitis

Identifiers

PMID37946776
PMCPMC10631407

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