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Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients with Cone-Rod Dystrophy and Amelogenesis Imperfecta

Hirji, N; Bradley, PD; Li, S; Vincent, A; Pennesi, ME; Thomas, AS; Heon, E; ... Michaelides, M; + view all (2018) Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients with Cone-Rod Dystrophy and Amelogenesis Imperfecta. American Journal of Ophthalmology , 188 pp. 123-130. 10.1016/j.ajo.2018.01.029. Green open access

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Abstract

The association of amelogenesis imperfecta (AI) with cone-rod dystrophy (CORD) was originally described in a consanguineous Arabic family with 29 affected members, who resided in the Gaza strip.1-3 The condition has been given the eponym Jalili Syndrome, after one of the authors who originally described the condition in 1988.

Type: Article
Title: Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients with Cone-Rod Dystrophy and Amelogenesis Imperfecta
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.ajo.2018.01.029
Publisher version: https://doi.org/10.1016/j.ajo.2018.01.029
Language: English
Additional information: This article published under a Creative Common CC BY 4.0 licence (https://creativecommons.org/licenses/by/4.0/)
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Ophthalmology
URI: https://discovery.ucl.ac.uk/id/eprint/10043561
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