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
11.
Corona-Rivera J, Zenteno J, Ordonez-Labastida V, Cruz-Cruz J, Cortes-Pastrana R, Pena-Padilla C, et al.
Eur J Med Genet
. 2023 Sep;
66(10):104826.
PMID: 37657631
MTSS2-related neurodevelopmental disorder (MTSS2-related NDD) (MIM 620086) is characterized by intellectual developmental disorder with ocular anomalies and distinctive facial features (IDDOF). The only existing report to date described five individuals...
12.
Macriz-Romero N, Vera-Duarte G, Guerrero-Becerril J, Chacon-Camacho O, Astiazaran M, Zenteno J, et al.
Int Ophthalmol
. 2023 Aug;
43(10):3659-3665.
PMID: 37542530
Purpose: To describe the ocular clinical characteristics of a group of Mexican patients with lamellar ichthyosis (LI) arising from TGM1 pathogenic variants. Methods: Ophthalmological exploration, pedigree analysis and genetic screening...
13.
Chacon-Camacho O, Arce-Gonzalez R, Sanchez-de la Rosa F, Uriostegui-Rojas A, Hofmann-Blancas M, Mata-Flores F, et al.
Curr Mol Med
. 2023 Jun;
24(10):1231-1249.
PMID: 37272463
Glaucoma is a group of diverse diseases characterized by cupping of the optic nerve head due to the loss of retinal ganglion cells. It is the most common cause of...
14.
Corona-Rivera J, Zenteno J, Lopez-Perez L, Yokoyama-Rebollar E, Villarroel C, Barragan-Arevalo T, et al.
Mol Syndromol
. 2023 Apr;
14(2):143-151.
PMID: 37064331
Introduction: -related neurodevelopmental disorder (related NDD) is caused by pathogenic variants in the gene and is characterized by a distinctive facial appearance, intellectual disability, speech delay, seizures, feeding difficulties, cryptorchidism,...
15.
Leal-Rodriguez R, Barragan-Arevalo T, Perez-Torres A, Giraldo-Gomez D, Zenteno J
Clin Dysmorphol
. 2023 Feb;
32(2):62-64.
PMID: 36779776
No abstract available.
16.
Kumari A, Ayala-Ramirez R, Zenteno J, Huffman K, Sasik R, Ayyagari R, et al.
Sci Rep
. 2022 Sep;
12(1):15273.
PMID: 36088481
Mutations in the Membrane-type frizzled related protein (Mfrp) gene results in an early-onset retinal degeneration associated with retinitis pigmentosa, microphthalmia, optic disc drusen and foveal schisis. In the current study,...
17.
Arce-Gonzalez R, Chacon-Camacho O, Ordonez-Labastida V, Graue-Hernandez E, Navas-Perez A, Zenteno J
Int Ophthalmol
. 2022 Sep;
43(3):807-815.
PMID: 36048286
Aim: To describe a family segregating a novel truncating ZNF469 homozygous mutation causing brittle cornea syndrome type 1 in a male patient and associated with corneal ectasia in his two...
18.
Ramirez-Garcia M, Davila-Ortiz de Montellano D, Martinez-Ruano L, Ochoa-Morales A, Romero-Hidalgo S, Zenteno J, et al.
Neurodegener Dis
. 2022 Aug;
22(1):34-42.
PMID: 35926480
Introduction: There are reports of different clinical statuses in carriers of intermediate alleles (IAs) of CAG trinucleotide repeats in the HTT gene, from individuals affected by a clinical picture indistinguishable...
19.
Arce-Gonzalez R, Chacon-Camacho O, Navas-Perez A, Gonzalez-Gonzalez M, Martinez-Aguilar A, Zenteno J
Ophthalmic Genet
. 2021 Nov;
43(2):224-229.
PMID: 34844512
Purpose: X-linked megalocornea (XMC) is a rare anterior segment malformation characterized by a nonprogressive enlargement of the cornea to 13 mm or greater in the setting of normal intraocular pressure....
20.
Chacon-Camacho O, Pozo-Molina G, Mendez-Catala C, Reyes-Reali J, Mendez-Cruz R, Zenteno J
Endocr Metab Immune Disord Drug Targets
. 2021 Feb;
22(2):198-211.
PMID: 33563162
Knowledge of epidemiology, genetic etiopathogenesis, diagnostic criteria, and management of familial hypercholesterolemia have increased in the last two decades. Several population studies have shown that familial hypercholesterolemia is more frequent...