Correlation Between Trabeculodysgenesis Assessed by Ultrasound Biomicroscopy and Surgical Outcomes in Primary Congenital Glaucoma.
Sign Up to like & getrecommendations! Published in 2018 at "American journal of ophthalmology"
DOI: 10.1016/j.ajo.2018.08.022
Abstract: PURPOSE To evaluate ultrasound biomicroscopy (UBM) characteristics of trabeculodysgenesis and explore its correlation with the outcomes of microcatheter-assisted trabeculotomy (MAT) in eyes with primary congenital glaucoma (PCG). DESIGN A prospective, interventional case series. METHODS Patients… read more here.
Keywords: trabeculodysgenesis; congenital glaucoma; primary congenital; type ... See more keywords
Caregiver Burden in Primary Congenital Glaucoma.
Sign Up to like & getrecommendations! Published in 2019 at "American journal of ophthalmology"
DOI: 10.1016/j.ajo.2019.05.003
Abstract: PURPOSE To evaluate the demographic, clinical, and socioeconomic factors associated with quality of life (QOL) in caregivers of children with primary congenital glaucoma (PCG) in south India. DESIGN Cross-sectional survey. METHODS Caregivers of children under… read more here.
Keywords: caregivers children; age; caregiver; congenital glaucoma ... See more keywords
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene.
Sign Up to like & getrecommendations! Published in 2018 at "Stem cell research"
DOI: 10.1016/j.scr.2018.01.004
Abstract: The human iPSC cell line, GLC-FiPS4F1 (ESi047-A), derived from dermal fibroblast from the patient with congenital glaucoma caused by the mutation of the gene CYP1B1, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC… read more here.
Keywords: caused mutation; line; congenital glaucoma; patient congenital ... See more keywords
Primary congenital glaucoma: An updated review
Sign Up to like & getrecommendations! Published in 2019 at "Saudi Journal of Ophthalmology"
DOI: 10.1016/j.sjopt.2019.10.002
Abstract: Primary congenital glaucoma (PCG) is a rare disease affecting children early in life. PCG was considered untreatable with inevitable blindness. However, recent advances in biochemical and genetic studies, the introduction of new diagnostic tools, intraocular… read more here.
Keywords: glaucoma updated; pcg; congenital glaucoma; updated review ... See more keywords
Ocular Aberrations in Eyes with Primary Congenital Glaucoma
Sign Up to like & getrecommendations! Published in 2022 at "Current Eye Research"
DOI: 10.1080/02713683.2022.2074045
Abstract: Abstract Purpose To highlight the magnitude of ocular higher order aberrations (HOA) and lower order aberrations (LOA), including component contributions from corneal and internal planes in Primary Congenital Glaucoma (PCG) patients. Methods Consecutive treated PCG… read more here.
Keywords: glaucoma; congenital glaucoma; pcg patients; corneal ... See more keywords
Illuminated Microcatheter Passage Assisted Circumferential Trabeculotomy and Trabeculectomy (IMPACTT): An improved surgical procedure for Primary Congenital Glaucoma
Sign Up to like & getrecommendations! Published in 2022 at "Seminars in Ophthalmology"
DOI: 10.1080/08820538.2022.2105150
Abstract: ABSTRACT Purpose To report an improved surgical procedure for primary congenital glaucoma (PCG). Case report An apparently healthy 4-month-old male child was referred by an ophthalmologist with the preliminary diagnosis of congenital glaucoma. Office examination… read more here.
Keywords: congenital glaucoma; improved surgical; surgical procedure; passage assisted ... See more keywords
CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma patients
Sign Up to like & getrecommendations! Published in 2017 at "Ophthalmic Genetics"
DOI: 10.1080/13816810.2016.1188121
Abstract: Primary congenital glaucoma (PCG) is a rare and severe autosomal recessive disease, characterized by high intraocular pressure during the neonatal or early infantile period. If undetected and timel... read more here.
Keywords: congenital glaucoma; mutational screening; primary congenital; screening portuguese ... See more keywords
Microphthalmia, Dermal Aplasia, and Sclerocornea Syndrome: Endoscopic Cyclophotocoagulation in the Management of Congenital Glaucoma
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Glaucoma"
DOI: 10.1097/ijg.0000000000000812
Abstract: Purpose: To report on the use of endoscopic cyclophotocoagulation (ECP) to treat congenital glaucoma in a triple X female with microphthalmia, dermal aplasia, and sclerocornea (MIDAS) syndrome. Observations: The patient demonstrated linear streaks on the… read more here.
Keywords: microphthalmia dermal; congenital glaucoma; glaucoma; endoscopic cyclophotocoagulation ... See more keywords
CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Glaucoma"
DOI: 10.1097/ijg.0000000000001132
Abstract: Purpose: To identify variants in the CYP1B1 gene in northeastern Brazilian patients with primary congenital glaucoma (PCG) and possible genotype-phenotype correlations. Materials and Methods: This is a cross-sectional observational study of 17 nonrelated patients with… read more here.
Keywords: cyp1b1 gene; gene; primary congenital; congenital glaucoma ... See more keywords
Neglected Congenital Glaucoma With Lens Coloboma
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Glaucoma"
DOI: 10.1097/ijg.0000000000001288
Abstract: Purpose: To report a case of lens coloboma in a case of neglected primary congenital glaucoma. Materials and Methods: A 5-year-old boy was brought by the parents with complaints of diminution of vision in both… read more here.
Keywords: lens coloboma; glaucoma lens; glaucoma; neglected congenital ... See more keywords
A Rare Case Report of Frank Ter Haar Syndrome in a Sibling Pair Presenting with Congenital Glaucoma.
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Glaucoma"
DOI: 10.1097/ijg.0000000000001420
Abstract: Frank Ter Haar Syndrome (FTHS) is a rare autosomal recessive disorder with characteristic skeletal, cardiac, ocular and craniofacial abnormalities. We report a sibling pair presenting with clinical features typical of FTHS, born to consanguineous parents,… read more here.
Keywords: haar syndrome; frank ter; sibling pair; glaucoma ... See more keywords