The incidence of strabismus and refractive error in patients with blepharophimosis, ptosis and epicanthus inversus syndrome (BPES)
Author:
Publisher
Informa UK Limited
Subject
Ophthalmology
Link
http://www.tandfonline.com/doi/pdf/10.1076/stra.11.3.173.16645
Reference11 articles.
1. Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22
2. Two Families with Blepharophimosis/Ptosis/Epicanthus Inversus Syndrome Have Mutations in the Putative Forkhead Transcription Factor FOXL2
3. FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation
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1. The Association between Refractive Errors and Congenital Ptosis;Iraqi Journal of Community Medicine;2024-01
2. Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family;BMC Ophthalmology;2023-11-07
3. Eyelid, Orbital, and Lacrimal Disorders in the Neonate;NeoReviews;2023-10-01
4. Application of e-PTFE Frontalis Suspension in the Treatment of Congenital Ptosis in Children;Frontiers in Surgery;2022-05-16
5. “Blepharophimosis‐plus” syndromes: Frequency of systemic genetic disorders that also include blepharophimosis;Clinical & Experimental Ophthalmology;2021-04-29
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