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.
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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 |
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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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