Morphometric evaluation of the foramen magnum for sex determination: A study from Saudi Arabia by Madadin, Mohammed, Menezes, Ritesh G, Al Saif, Hind, Abo Alola, Hossain, Al Muhanna, Afnan, Gullenpet, Abid H, Nagesh, K.R, Kharoshah, Magdy A, Al Dhafery, Bander

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A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American by Dougherty, Sean C, Harper, Amy, Al Saif, Hind, Vorona, Gregory, Haines, Scott R

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Uterine and tubal abnormalities in infertile Saudi Arabian women: A teaching hospital experience by Al-Turki, Haifa, Gullenpet, Abid, Syed, Anjum, Al-Saif, Hind, Aldhafery, Bander

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A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations by Saif, Hind Al, Kanhere, Mansi, Wallace, Michael, Sahni, Dev R., Couser, Natario L.

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Unusual Presentation of Gianotti-Crosti Syndrome due to Epstein-Barr Virus Infection by Al Kaabi, Salwa, Al Kaabi, Aysha, Kara Hamo, Yasmin, Al Kaabi, Amani, Al Dhaheri, Hind Saif, Al Tatari, Hossam

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Multiloculated Cavitary Primary Pulmonary Hodgkin Lymphoma: Case Series by Aljehani, Yasser, Al-Saif, Hind, Al-Osail, Aisha, Al-Osail, Emad

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Case report of mosaic creatine transporter deficiency in a male pediatric patient by Brooks, Amy, Al Saif, Hind, McDermott, Emily

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Ocular Manifestations of the NAA10-Related Syndrome by Couser, Natario L., Lent, Jennifer M., Saif, Hind Al, Gupta, Angela S.

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Ophthalmologic and facial abnormalities of Nicolaides-Baraitser syndrome by Simmers, Russell, Goodwin, Allison, Al Saif, Hind, Couser, Natario

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Eye, ocular adnexa, and facial manifestations of tetrasomy 18p: case report and literature review by Saadeh-Jackson, Stephanie, King, Kayla, Al Saif, Hind, Jackson-Cook, Colleen, Couser, Natario

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eP101 - Eye, ocular adnexa, and facial manifestations of tetrasomy 18p: case report and literature review by Saadeh-Jackson, Stephanie, King, Kayla, Al Saif, Hind, Jackson-Cook, Colleen, Couser, Natario

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Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review by Babu, Kevin, Seamon, Kimberly, Jewell, Ann, Harrison, Anna, Harper, Amy, Al Saif, Hind, Couser, Natario

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Eye and ocular adnexa manifestations of MED12 -related disorders by Shah, Arth, Bapna, Monika, Al-Saif, Hind, Li, Rachel, Couser, Natario L

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Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay by Tan, Senwei, Zhang, Qiumeng, Zhan, Rui, Luo, Si, Han, Yaoling, Yu, Bin, Muss, Candace, Pingault, Veronique, Marlin, Sandrine, Delahaye, Andrée, Peters, Sophia, Perne, Claudia, Kreiß, Martina, Spataro, Nino, Trujillo-Quintero, Juan Pablo, Racine, Caroline, Tran-Mau-Them, Frederic, Phornphutkul, Chanika, Besterman, Aaron D, Martinez, Julian, Wang, Xiuxia, Tian, Xiaoyu, Srivastava, Siddharth, Urion, David K, Madden, Jill A, Saif, Hind Al, Morrow, Michelle M, Begtrup, Amber, Li, Xing, Jurgensmeyer, Sarah, Leahy, Peter, Zhou, Shimin, Li, Faxiang, Hu, Zhengmao, Tan, Jieqiong, Xia, Kun, Guo, Hui

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De novo variants in DENND5B cause a neurodevelopmental disorder by Scala, Marcello, Ferla, Matteo, Fatemi, Ali, Phillips, John A., Rio, Marlene, Siquier, Karine, Musante, Ilaria, Baldassari, Simona, Iacomino, Michele, Acosta, Maria T., Allworth, Aimee, Afzali, Ben, Bademci, Guney, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, HsiaoTuan, Chinn, Ivan, Clark, Gary D., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Fisher, Paul G., Fogel, Brent L., Gahl, William A., Glass, Ian, Godfrey, Rena A., Grajewski, Alana, Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, Hom, Jason, Huang, Alden, Introne, Wendy, Jarvik, Jeffrey, Jobanputra, Vaidehi, Kilich, Gonench, Kohler, Jennefer N., Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Marth, Gabor, Martin, Beth A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo, Morimoto, Marie, Nakano-Okuno, Mariko, Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Parker, Neil H., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Saporta, Mario, Schaechter, Judy, Seto, Elaine, Shelkowitz, Emily, Shin, Jimann, Solnica-Krezel, Lilianna, Sweetser, David A., Sybert, Virginia, Tarakad, Arjun, Velinder, Matt, Viskochil, Dave, Ward, Patricia A., Wegner, Daniel, Weisz Hubshman, Monika, Wener, Mark, Wenger, Tara, Reed, Sara, Al Saif, Hind, Walsh, Matthew B., Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Severino, Mariasavina

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Demographics and co‐occurring conditions in a clinic‐based cohort with Down syndrome in the United Arab Emirates by Corder, Jennifer Price, Al Ahbabi, Fatima Jaber Sehmi, Al Dhaheri, Hind Saif, Chedid, Fares

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Ophthalmologic and facial abnormalities of Nicolaides-Baraitser syndrome by Simmers, Russell, Goodwin, Allison, Al Saif, Hind, Couser, Natario

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Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review by Babu, Kevin, Seamon, Kimberly, Jewell, Ann, Harrison, Anna, Harper, Amy, Al Saif, Hind, Couser, Natario

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Eye and ocular adnexa manifestations of MED12-related disorders by Shah, Arth, Bapna, Monika, Al-Saif, Hind, Li, Rachel, Couser, Natario L.

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Ocular Manifestations of the NAA10-Related Syndrome by Gupta, Angela S, Saif, Hind Al, Lent, Jennifer M, Couser, Natario L

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