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Quoted phrase not found in phrase index: "Familial congenital nasolacrimal duct obstruction"
Page 1
Bony Congenital Nasolacrimal Duct Obstruction: A Novel Phenotype of Aplasia of Lacrimal and Major Salivary Glands.
Feng ZX, Liu W, Li Z, Cui Y, Li L, Zhang C. Feng ZX, et al. Ophthalmology. 2024 May;131(5):589-594. doi: 10.1016/j.ophtha.2023.12.003. Epub 2023 Dec 9. Ophthalmology. 2024. PMID: 38081329
Reported ophthalmic manifestations of ALSG include aplasia of lacrimal glands, punctal agenesis, lacrimal sac mucocele, and membranous congenital nasolacrimal duct obstruction (CNLDO). ...PARTICIPANTS: Three Chinese families with b …
Reported ophthalmic manifestations of ALSG include aplasia of lacrimal glands, punctal agenesis, lacrimal sac mucocele, and me …
Office- or Facility-Based Probing for Congenital Nasolacrimal Duct Obstruction: A Report by the American Academy of Ophthalmology.
Morrison DG, Binenbaum G, Chang MY, Heidary G, Trivedi RH, Galvin JA, Pineles SL. Morrison DG, et al. Ophthalmology. 2021 Jun;128(6):920-927. doi: 10.1016/j.ophtha.2020.10.028. Epub 2020 Dec 24. Ophthalmology. 2021. PMID: 33358412 Review.
PURPOSE: To review the published literature assessing the efficacy and safety of in-office probing compared with facility-based probing to treat congenital nasolacrimal duct obstruction (NLDO). METHODS: Literature searches were conducted in March 2020 …
PURPOSE: To review the published literature assessing the efficacy and safety of in-office probing compared with facility-based probing to t …
Lacrimal outflow dysgenesis.
Yuen SJ, Oley C, Sullivan TJ. Yuen SJ, et al. Ophthalmology. 2004 Sep;111(9):1782-90. doi: 10.1016/j.ophtha.2004.02.011. Ophthalmology. 2004. PMID: 15350337
PARTICIPANTS: Fifty patients with lacrimal dysgenesis managed between 1992 and 2003. TESTING/INTERVENTION: The diagnosis of lacrimal outflow dysgenesis was made based on the following criteria: absent or hypoplastic punctum, canaliculus, lacrimal sac, and …
PARTICIPANTS: Fifty patients with lacrimal dysgenesis managed between 1992 and 2003. TESTING/INTERVENTION: The diagnosis of lacrim …
The Evolving Story of CNLDO: Serial Photographic Documentation and Parental Perspectives.
Singh S, Ali MJ. Singh S, et al. Ophthalmic Plast Reconstr Surg. 2023 Jan-Feb 01;39(1):88-91. doi: 10.1097/IOP.0000000000002242. Epub 2022 Jul 13. Ophthalmic Plast Reconstr Surg. 2023. PMID: 35829659
PURPOSE: The purpose of this study is to report the temporal sequence of symptomatology of bilateral congenital nasolacrimal duct obstruction and parental perspectives of 2 established lacrimal surgeons studying the natural history of their newb …
PURPOSE: The purpose of this study is to report the temporal sequence of symptomatology of bilateral congenital nasolacrimal …
A case of blepharophimosis: Freeman Sheldon syndrome.
Bowman S, Noble G, Rahmani B, Mets M, Ralay Ranaivo H, Castelluccio V. Bowman S, et al. Ophthalmic Genet. 2022 Feb;43(1):130-133. doi: 10.1080/13816810.2021.1989603. Epub 2021 Oct 19. Ophthalmic Genet. 2022. PMID: 34664542
Although the mode of inheritance for Freeman Sheldon syndrome (formerly known as Whistling Face Syndrome) is often autosomal dominant, our patient had no known family history of congenital abnormalities or consanguinity. However, genetic testing confirmed a heterozy …
Although the mode of inheritance for Freeman Sheldon syndrome (formerly known as Whistling Face Syndrome) is often autosomal dominant, our p …
A symptom survey and quality of life questionnaire for nasolacrimal duct obstruction in children.
Holmes JM, Leske DA, Cole SR, Chandler DL, Repka MX; Nasolacrimal Duct Obstruction Questionnaire Study Group; Silbert DI, Tien DR, Bradley EA, Sala NA, Levin EM, Hoover DL, Klimek DL, Mohney BG, Laby DM, Lee KA, Enzenauer RW, Bacal DA, Mills MD, Beck RW; Pediatric Eye Disease Investigator Group. Holmes JM, et al. Ophthalmology. 2006 Sep;113(9):1675-80. doi: 10.1016/j.ophtha.2006.03.041. Epub 2006 Jul 7. Ophthalmology. 2006. PMID: 16828516 Free PMC article.
PURPOSE: To develop and validate a new parental questionnaire addressing symptoms and health-related quality of life (HRQL) in childhood nasolacrimal duct obstruction (NLDO). DESIGN: Cross-sectional study. ...MAIN OUTCOME MEASURE: The NLDO questionnaire sc …
PURPOSE: To develop and validate a new parental questionnaire addressing symptoms and health-related quality of life (HRQL) in childhood …
Prevalence of childhood ocular morbidity in a peri-urban setting in Bangladesh: a community-based study.
Hussain AHME, Roy T, Ferdausi N, Sen U. Hussain AHME, et al. Public Health. 2019 May;170:103-112. doi: 10.1016/j.puhe.2019.02.026. Epub 2019 Apr 13. Public Health. 2019. PMID: 30991172
The prevalence of ocular morbidity and childhood blindness were 5.63% (95% confidence interval [CI] = 5.27-6.16) and 0.060% (95% CI = 0.03-0.11), respectively. The most commonly observed ocular morbidities were refractive error (3.24%; 95% CI = 3.11-3.45), allergic eye con …
The prevalence of ocular morbidity and childhood blindness were 5.63% (95% confidence interval [CI] = 5.27-6.16) and 0.060% (95% CI = 0.03-0 …
Prevalence and Risk Factors of Amblyopia among Refractive Errors in an Eastern European Population.
Mocanu V, Horhat R. Mocanu V, et al. Medicina (Kaunas). 2018 Mar 20;54(1):6. doi: 10.3390/medicina54010006. Medicina (Kaunas). 2018. PMID: 30344237 Free PMC article.
Parents participated in a face-to-face interview. The questionnaire contained details about their family history of amblyopia; the child's maternal nutritional status in the preconception period; their history of maternal smoking or work in a toxic environment; the child's …
Parents participated in a face-to-face interview. The questionnaire contained details about their family history of amblyopia; the ch …
New autosomal dominant branchio-oculo-facial syndrome.
Fujimoto A, Lipson M, Lacro RV, Shinno NW, Boelter WD, Jones KL, Wilson MG. Fujimoto A, et al. Am J Med Genet. 1987 Aug;27(4):943-51. doi: 10.1002/ajmg.1320270422. Am J Med Genet. 1987. PMID: 3321995 Review.
We observed an autosomal dominant disorder of abnormal upper lip, which resembles a poorly repaired cleft lip, malformed nose with broad bridge and flattened tip, lacrimal duct obstruction, malformed ears, and branchial cleft sinuses and/or linear skin …
We observed an autosomal dominant disorder of abnormal upper lip, which resembles a poorly repaired cleft lip, malformed nose with br …
Functional characterization of a novel TP63 mutation in a family with overlapping features of Rapp-Hodgkin/AEC/ADULT syndromes.
Serra V, Castori M, Paradisi M, Bui L, Melino G, Terrinoni A. Serra V, et al. Am J Med Genet A. 2011 Dec;155A(12):3104-9. doi: 10.1002/ajmg.a.34335. Epub 2011 Nov 8. Am J Med Genet A. 2011. PMID: 22069181 Free PMC article.
Some analyses suggest a relationship of the mutation site to the observed clinical picture, although this link is inconsistent. This suggests an appreciable phenotypic continuity within the TP63-related disorders. We report a 3-month-old boy ascertained for congenital …
Some analyses suggest a relationship of the mutation site to the observed clinical picture, although this link is inconsistent. This …