Corneal Crystals as an Initiating Factor for a Systemic Bone Marrow Transplant von Miller, Kelly, Iuorno, Joseph, Couser, Natario L

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Magnetic Resonance Imaging Findings and Genetic Testing Results in Children With Congenital Corneal Opacities von Xia, Julia L., Kadom, Nadja, Mansukhani, Sasha A., Couser, Natario L., Lenhart, Phoebe D.

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P376: A pediatric patient with a novel duplication of 1q21.2 to 1q25.3: A case report von Pan, Stephanie, Couser, Natario

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P408: Vision and enamel anomalies in Jalili syndrome: Case study and genetic insights von Choi, Jane, Couser, Natario

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The First Cataract Surgeons in the British Isles von Leffler, Christopher T., Schwartz, Stephen G., Peterson, Eric, Couser, Natario L., Salman, Abdul-Rahman

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C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases von Shinbashi, Meagan, Jewell, Ann, Randolph, Jessica, Couser, Natario

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NPHP1‐Related ciliopathies: A new case and major review of the ophthalmic manifestations of 147 reported cases von Reddy, Shivania, Simmers, Russell, Shah, Arth, Couser, Natario

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P397: A case of congenital myasthenic syndrome with AChR deficiency due to biallelic variants in CHRNE gene von Batheja, Aashish, Bayer-Vile, Julie, Silverstein, Evan, Couser, Natario

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Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases von Kumar, Virang, Pandya, Arti, Couser, Natario L.

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P267: The essential role of genetic testing in the phenotypic heterogeneity of Stargardt disease von Nalamalapu, Rithvik, Bayer-Vile, Julie, Leffler, Christopher, Peplow, Katherine, Randolph, Jessica, Couser, Natario

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Bietti’s crystalline dystrophy in an African American patient: an unusual racial demographic for a condition more common in individuals of East Asian descent von Kumar, Virang, Prell, Jordyn, Jewell, Ann, Couser, Natario

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Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review von Stingl, Cybil S., Couser, Natario L., Jackson-Cook, Colleen

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Augmented Hummelsheim procedure to treat complete abducens nerve palsy von Couser, Natario L., MD, Lenhart, Phoebe D., MD, Hutchinson, Amy K., MD

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Cleft palate and hypopituitarism in a patient with Noonan‐like syndrome with loose anagen hair‐1 von Couser, Natario L., Keelean‐Fuller, Debra, Davenport, Marsha L., Haverfield, Eden, Masood, Maheer M., Henin, Mark, Aylsworth, Arthur S.

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Corrigendum #2 to “Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review” von Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.

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Ophthalmia neonatorum due to Escherichia coli: A rare cause or an emerging bacterial etiology of neonatal conjunctivitis? von Saadeh‐Jackson, Stephanie, Rodriguez, Linnet, Leffler, Christopher T., Freymiller, Casey, Wolf, Elizabeth, Wijesooriya, Niran, Couser, Natario L.

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An Adult Loa loa Worm in the Upper Eyelid: An Atypical Presentation of Loiasis in the United States von Rodriguez, Linnet, White, Julia Michelle, Richards, Nikisha Q., You, Alan X., Couser, Natario L.

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Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutation von Couser, Natario L., Pande, Chetna K., Turcott, Christie M., Spector, Elaine B., Aylsworth, Arthur S., Powell, Cynthia M.

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The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review von Couser, Natario L., Masood, Maheer M., Strande, Natasha T., Foreman, Ann Katherine M., Crooks, Kristy, Weck, Karen E., Lu, Mei, Wilhelmsen, Kirk C., Roche, Myra, Evans, James P., Berg, Jonathan S., Powell, Cynthia M.

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Camptodactyly and the 22q11.2 deletion syndrome von Couser, Natario L., Pande, Chetna K., Walsh, Jonathan M., Tepperberg, James, Aylsworth, Arthur S.

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