Cargando…

Visual deficits in Nepalese patients with oculocutaneous albinism

BACKGROUND: Albinism poses a significant threat to visual functions and causes remarkable ocular morbidity often resulting in visual disabilities. The study aimed at describing the visual status in patients with diagnosed cases of complete oculocutaneous albinism (OCA) attending to a tertiary eye ho...

Descripción completa

Detalles Bibliográficos
Autores principales:	Khanal, Safal, Pokharel, Amrit, Kandel, Himal
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2016
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812000/ https://www.ncbi.nlm.nih.gov/pubmed/25823539 http://dx.doi.org/10.1016/j.optom.2015.01.002

Ejemplares similares

Oculocutaneous albinism
por: Grønskov, Karen, et al.
Publicado: (2007)

Retinopathy of prematurity in oculocutaneous albinism
por: Chandra, Parijat, et al.
Publicado: (2019)

The Coexistence of Oculocutaneous Albinism with Schizophrenia
por: Tsai, Alicia L, et al.
Publicado: (2020)

Quality of life in patients with oculocutaneous albinism
por: Maia, Marcus, et al.
Publicado: (2015)

Effects of spectacles and telescopes on visual function in students with oculocutaneous albinism
por: Jhetam, Siddeeqa, et al.
Publicado: (2020)

Genetic analyses of Vietnamese patients with oculocutaneous albinism
por: Thuong, Ma Thi Huyen, et al.
Publicado: (2022)

Oculocutaneous albinism in a Puerto Rican patient
por: Bindernagel, Richard, et al.
Publicado: (2023)

Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
por: Chan, Hwei Wuen, et al.
Publicado: (2021)

Visual rehabilitation of people with oculocutaneous albinism in a tertiary clinical setting in Pakistan
por: Shah, Mufarriq, et al.
Publicado: (2020)

Genetic Causes of Oculocutaneous Albinism in Pakistani Population
por: Sajid, Zureesha, et al.
Publicado: (2021)

Multimodal imaging of fovea plana in oculocutaneous albinism
por: Singh, Simar R, et al.
Publicado: (2019)

Presentation of Autism in a child with Oculocutaneous Albinism
por: Gokul Raj, M, et al.
Publicado: (2022)

Abnormal foveal morphology in carriers of oculocutaneous albinism
por: Kuht, Helen J, et al.
Publicado: (2023)

Refractive errors in Cameroonians diagnosed with complete oculocutaneous albinism
por: Eballé, André Omgbwa, et al.
Publicado: (2013)

Dermoscopy of Amelanotic Melanoma in a Patient With Oculocutaneous Albinism
por: Uyar, Belkis, et al.
Publicado: (2020)

Evident hypopigmentation without other ocular deficits in Dutch patients with oculocutaneous albinism type 4
por: Kruijt, C. C., et al.
Publicado: (2021)

Phenotypic variations in ocular features among siblings with oculocutaneous albinism
por: Bhate, Manjushree, et al.
Publicado: (2022)

Mutational Analysis of Oculocutaneous Albinism: A Compact Review
por: Kamaraj, Balu, et al.
Publicado: (2014)

Mutation analysis of a Chinese family with oculocutaneous albinism
por: Wang, Xiong, et al.
Publicado: (2016)

Maple Syrup Urine Disease and Oculocutaneous Albinism in Twins
por: Nagabushana, Divya, et al.
Publicado: (2014)

Ophthalmological Manifestations of Oculocutaneous and Ocular Albinism: Current Perspectives
por: Neveu, Magella M, et al.
Publicado: (2022)

Oculocutaneous albinism: the neurological, behavioral, and neuro-ophthalmological perspective
por: Galli, Jessica, et al.
Publicado: (2023)

Multiple Basal Cell Carcinomas in a Patient of Oculocutaneous Albinism
por: Behera, Debasmita, et al.
Publicado: (2017)

Eccrine Porocarcinoma with Squamous Differentiation in a Patient with Oculocutaneous Albinism
por: Dey, Biswajit, et al.
Publicado: (2020)

Black Piedra in an Amerindian Girl with Oculocutaneous Albinism Type 2
por: Piquero-Casals, Jaime, et al.
Publicado: (2023)

Management of complicated proliferative diabetic retinopathy in a patient with oculocutaneous albinism
por: Marshood, Abdullah Al, et al.
Publicado: (2022)

Resistant schizophrenia in a patient with oculocutaneous albinism successfully treated with clozapine
por: Jelti, A., et al.
Publicado: (2022)

Characterization of Temperature-Dependent Kinetics of Oculocutaneous Albinism-Causing Mutants of Tyrosinase
por: Wachamo, Samuel A., et al.
Publicado: (2021)

Lack of adequate sun protection for children with oculocutaneous albinism in South Africa
por: Lund, Patricia M, et al.
Publicado: (2008)

Nonhuman Primate Model of Oculocutaneous Albinism with TYR and OCA2 Mutations
por: Wu, Kun-Chao, et al.
Publicado: (2020)

Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism
por: Xu, Chenyang, et al.
Publicado: (2020)

Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population
por: Jaworek, Thomas J, et al.
Publicado: (2012)

Mutational analysis of a Chinese family with oculocutaneous albinism type 2
por: Wang, Xiong, et al.
Publicado: (2017)

Genetic Analysis of 28 Chinese Families With Tyrosinase-Positive Oculocutaneous Albinism
por: Ma, Linya, et al.
Publicado: (2021)

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences
por: Kruijt, Charlotte C., et al.
Publicado: (2022)

Determining a Worldwide Prevalence of Oculocutaneous Albinism: A Systematic Review
por: Kromberg, Jennifer G. R., et al.
Publicado: (2023)

An unusual combination of Unilateral Orbital Plexiform Neurofibroma in a patient with oculocutaneous albinism
por: Saravanan, J, et al.
Publicado: (2014)

Low-vision intervention for oculocutaneous albinism in a Tertiary Eye Care Hospital in India
por: Gopalakrishnan, Sarika, et al.
Publicado: (2023)

Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism
por: KO, JUNG MIN, et al.
Publicado: (2012)

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population
por: Shahzad, Mohsin, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_g7rh9vtnrcnaf33pjjo0uliof8