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About 163 results

ALLMedicine™ Peters Anomaly Center

Research & Reviews  63 results

Outcomes of combined endoscopic vitrectomy and posteriorly placed glaucoma drainage dev...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976343
BMC Ophthalmology; Jacobson A, Besirli CG et. al.

Apr 3rd, 2022 - This study aims to describe outcomes of posteriorly-placed glaucoma drainage devices (GDD) with concurrent endoscopic vitrectomy in pediatric patients with glaucoma and corneal opacification. This retrospective case series identified patients unde...

The 2021 Congress of the International Society for Twin Studies: Twin Research at the C...
https://doi.org/10.1017/thg.2022.4
Twin Research and Human Genetics : the Official Journal O... Segal NL, Pratt-Thompson E

Feb 24th, 2022 - Selected highlights from the 2021 Congress of the International Society for Twin Studies are reviewed. The perspectives of a new graduate student member to the society are also included. Timely research covering issues related to maternal bonding ...

Long-term Experience and Visual Acuity Outcomes in Patients With Peters Anomaly.
https://doi.org/10.3928/01913913-20210412-01
Journal of Pediatric Ophthalmology and Strabismus; Donoso Rojas R, Jara Urrutia G et. al.

Oct 1st, 2021 - To report the results from a cases series of patients with Peters anomaly and propose management and treatment approaches according to the alterations associated with each case. The records of 27 patients (32 eyes) clinically diagnosed as having P...

T-cell Lymphoblastic Lymphoma in a Patient With Chromosome 8q21.11 Microdeletion.
https://doi.org/10.1097/MPH.0000000000002309
Journal of Pediatric Hematology/oncology; Yip J, Thompson KS

Sep 7th, 2021 - The chromosome 8q21.11 deletion syndrome is an extremely rare genetic condition characterized by facial dysmorphic features, Peters anomaly and impaired intellectual development. We report a case of a 2-year-old female with chromosome 8q21.11-q21....

Phenotypic Spectrum of Peters Anomaly: Implications for Management.
https://doi.org/10.1097/ICO.0000000000002768 10.1097/ICO.0000000000002577
Cornea Elbaz U, Ali A et. al.

Jun 29th, 2021 - The aim of this study was to characterize the wide phenotypic spectrum of Peters anomaly and to suggest a management algorithm based on disease phenotype. The charts of all children diagnosed with Peters anomaly between January 2000 and December 2...

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News  2 results

Antimalarials in Pregnancy: Baby's Ocular Problems Rare
https://www.medpagetoday.com/rheumatology/lupus/76304

Nov 13th, 2018 - Infants born to mothers who were being treated with antimalarial drugs during pregnancy had a "low to nonexistent" risk of ocular abnormalities, a systematic literature review suggested. In studies that included 1,477 infants, there were two cases...

An Infant With Leukocoria
https://www.medscape.com/viewarticle/759475_4

Mar 6th, 2012 - Discussion Peters anomaly is a rare congenital disorder associated with a wide spectrum of clinical manifestations, ranging from unilateral isolated corneal opacification to bilateral cases that present with cataracts, glaucoma, and systemic malfo...

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