Juan Carlos Zenteno
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Explore the profile of Juan Carlos Zenteno including associated specialties, affiliations and a list of published articles.
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87
Citations
579
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Recent Articles
1.
Rosales-Padron J, Chacon-Camacho O, Ordonez-Labastida V, Ledesma-Gil G, Graue-Wiechers F, Zenteno J
Ophthalmic Genet
. 2025 Mar;
:1-6.
PMID: 40044626
Objective: Angioid streaks (AS) are uncommon retinal lesions associated with significant risk of vision loss due to choroidal neovascularization. About half of AS cases have a concurrent disease, most commonly...
2.
Chacon-Camacho O, Flores-Lagunes L, Small K, Udar N, Udar U, Diaz A, et al.
Mol Vis
. 2025 Feb;
30:400-408.
PMID: 39959174
Purpose: North Carolina macular dystrophy (NCMD) is a rare autosomal dominantly inherited congenital maculopathy caused by either non-coding point mutations or tandem duplications in the DNase I hypersensitivity site DHS6S1,...
3.
Diazceballos-Garcia A, Matsui R, Chairez Miranda M, Rosales Padron J, Graue-Wiechers F, Zenteno J
Int Ophthalmol
. 2024 Dec;
45(1):1.
PMID: 39644342
Purpose: Description of retinal phenotype by structural and functional testing, ornithine plasma levels and mutational data of OAT gene in patients with Gyrate Atrophy (GA). Methods: Ophthalmologic examination, fundus photography...
4.
Chacon-Camacho O, Ordaz-Robles T, Cid-Garcia M, Yepes-Rodriguez O, Arce-Gonzalez R, Martinez-Aguilar A, et al.
Am J Med Genet A
. 2024 Sep;
197(1):e63869.
PMID: 39264138
Doyne honeycomb retinal dystrophy (DHRD), also termed malattia leventinese (MLVT), is a dominantly inherited ocular disease characterized by the progressive accumulation of macular and peripapillary drusenoid material beneath the retinal...
5.
Chacon-Camacho O, Xilotl-de Jesus N, Calderon-Martinez E, Ordonez-Labastida V, Neria-Gonzalez M, Villafuerte-de la Cruz R, et al.
Mol Genet Genomics
. 2024 Aug;
299(1):79.
PMID: 39162841
The purpose of this study was to analyze and molecularly describe the largest group of patients with ABCA4-associated retinal degeneration in Latin America. Pathogenic variants in ABCA4, a member of...
6.
Chacon-Camacho O, Ordaz-Robles T, Cid-Garcia M, Hofmann-Blancas M, Ledesma-Gil J, Garcia-Huerta M, et al.
Am J Med Genet A
. 2024 Jun;
194(10):e63716.
PMID: 38847211
Primary congenital glaucoma (PCG) is one of the leading causes of visual damage and blindness, severely affecting the quality of life of affected children. It is characterized by cupping of...
7.
Ruiz-Chavolla D, Barragan-Arevalo T, Cortes-Munoz D, Sanchez-Ruiz J, Zenteno J, Ledesma-Gil G
Ophthalmic Genet
. 2024 Mar;
45(3):299-302.
PMID: 38526149
Introduction: Alagille syndrome (AGS) is a genetic disease with multisystemic affection, including ocular manifestations. Recently, a high frequency of posterior segment findings, including macular changes, has been reported. This publication...
8.
Corona-Rivera J, Rios-Flores I, Zenteno J, Pena-Padilla C, Castillo-Reyes K, Bobadilla-Morales L, et al.
Mol Syndromol
. 2024 Feb;
15(1):51-57.
PMID: 38357259
Introduction: To our knowledge, there are few examples of intrafamilial variability involving two different -linked morphopathies within a same family. Here, we describe a Mexican family in which the son...
9.
Mora-Roldan G, Nava J, Gazarian K, Zenteno J
Stem Cell Res
. 2024 Jan;
75:103309.
PMID: 38217995
Retinitis pigmentosa (RP) is the most common retinal degeneration in humans and is characterized by the progressive degeneration of rods and cones and retinal pigment epithelium. We generated the IOCVi001-A...
10.
Fuentes-Nava A, Fierro-Arias L, Zenteno J, Apam-Garduno D
Clin Exp Dermatol
. 2023 Nov;
49(4):441-443.
PMID: 37942851
No abstract available.