Cargando…

Analysis of macular cone photoreceptors in a case of occult macular dystrophy

PURPOSE: To investigate changes in cone photoreceptors with adaptive optics (AO) fundus imaging and spectral domain optical coherence tomography (SD-OCT) in a case of occult macular dystrophy (OMD). PATIENT AND METHODS: Both eyes of a 42-year-old woman diagnosed with OMD were examined. We used an AO...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tojo, Naoki, Nakamura, Tomoko, Ozaki, Hironori, Oka, Miyako, Oiwake, Toshihiko, Hayashi, Atsushi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659265/ https://www.ncbi.nlm.nih.gov/pubmed/23696695 http://dx.doi.org/10.2147/OPTH.S44446

Ejemplares similares

Adaptive optics fundus images of cone photoreceptors in the macula of patients with retinitis pigmentosa
por: Tojo, Naoki, et al.
Publicado: (2013)

Occult Macular Dystrophy
por: Sayman Muslubaş, Işıl, et al.
Publicado: (2016)

Hydroxychloroquine's Early Impact on Cone Density
por: Ueda-Consolvo, Tomoko, et al.
Publicado: (2021)

Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy
por: Huchzermeyer, Cord, et al.
Publicado: (2023)

Detailed analyses of microstructure of photoreceptor layer at different severities of occult macular dystrophy by ultrahigh-resolution SD-OCT
por: Tsunoda, Kazushige, et al.
Publicado: (2022)

Intraoperative Changes in Idiopathic Macular Holes by Spectral-Domain Optical Coherence Tomography
por: Hayashi, Atsushi, et al.
Publicado: (2011)

Clinical and Genetic Characteristics of Chinese Patients with Occult Macular Dystrophy
por: Wang, Dan-Dan, et al.
Publicado: (2020)

PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHY
por: Scoles, Drew, et al.
Publicado: (2017)

Detection of photoreceptor disruption by adaptive optics fundus imaging and Fourier-domain optical coherence tomography in eyes with occult macular dystrophy
por: Kitaguchi, Yoshiyuki, et al.
Publicado: (2011)

Pattern-reversal visual-evoked potential in patients with occult macular dystrophy
por: Hanazono, Gen, et al.
Publicado: (2010)

Long-term changes of retinal pigment epithelium in the eyes with Vogt-Koyanagi-Harada disease observed by adaptive optics imaging
por: Nakamura, Tomoko, et al.
Publicado: (2019)

Two siblings with late-onset cone–rod dystrophy and no visible macular degeneration
por: Sakuramoto, Hiroyuki, et al.
Publicado: (2013)

Genetic characteristics of 234 Italian patients with macular and cone/cone-rod dystrophy
por: Falsini, Benedetto, et al.
Publicado: (2022)

Cone photoreceptor macular function and recovery after photostress in early non-exudative age-related macular degeneration
por: Rodriguez, John D, et al.
Publicado: (2018)

Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy
por: Birtel, Johannes, et al.
Publicado: (2018)

Hypotrichosis with Juvenile Macular Dystrophy
por: Almeida, Filipa Tavares, et al.
Publicado: (2018)

Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations
por: Manes, Gaël, et al.
Publicado: (2017)

Posterior microphthalmos with good visual acuity: A case report
por: Mihara, Miharu, et al.
Publicado: (2019)

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms
por: Kabuto, Takenori, et al.
Publicado: (2012)

Utility of en-face imaging in diagnosis of occult macular dystrophy with RP1L1 mutation: A case series
por: Ruan, Merry ZC., et al.
Publicado: (2019)

Concurrent Macular Corneal Dystrophy and Keratoconus
por: Mohammad-Rabei, Hossein, et al.
Publicado: (2012)

Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations
por: Cideciyan, Artur V., et al.
Publicado: (2022)

Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3
por: Ahn, Seong Joon, et al.
Publicado: (2022)

Structural and functional evaluation of macula in a 9-year-old boy with occult macular dystrophy and his affected elder sibling
por: Padhi, Tapas Ranjan, et al.
Publicado: (2016)

Rare occult macular dystrophy with a pathogenic variant in the RP1L1 gene in a patient of Swiss descent
por: Zabek, Olga, et al.
Publicado: (2022)

Bilateral coexistence of keratoconus and macular corneal dystrophy
por: Al-Hamdan, Ghazi, et al.
Publicado: (2009)

Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family
por: Qi, Yu-He, et al.
Publicado: (2017)

Electrophysiological Evaluation of Macular Dystrophies
por: Chiang, Tsun-Kang, et al.
Publicado: (2023)

Novel GUCA1A Mutations Suggesting Possible Mechanisms of Pathogenesis in Cone, Cone-Rod, and Macular Dystrophy Patients
por: Kamenarova, Kunka, et al.
Publicado: (2013)

Multimodal imaging evaluation of occult macular dystrophy associated with a novel RP1L1 variant
por: Bianco, Lorenzo, et al.
Publicado: (2022)

Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
por: Yang, Shaoqing, et al.
Publicado: (2023)

Outcome of Macular Hole Surgery in Bietti Crystalline Dystrophy
por: Nourinia, Ramin, et al.
Publicado: (2017)

Multicolor Imaging Characteristics of Best's Vitelliform Macular Dystrophy
por: Saurabh, Kumar, et al.
Publicado: (2019)

Laser-Induced Maculopathy Masquerading as Hereditary Macular Dystrophy
por: Al Adel, Fadwa, et al.
Publicado: (2021)

Large, Spontaneous Macular Hole with Posterior Pole Detachment in a Patient with Best Vitelliform Macular Dystrophy
por: Peart, Shamfa, et al.
Publicado: (2019)

The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy
por: Zhu, Zhe, et al.
Publicado: (2022)

Cone Photoreceptor Irregularity on Adaptive Optics Scanning Laser Ophthalmoscopy Correlates With Severity of Diabetic Retinopathy and Macular Edema
por: Lammer, Jan, et al.
Publicado: (2016)

Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics Imaging
por: Liu, Tao, et al.
Publicado: (2022)

Occult choroidal neovascularization after successful macular hole surgery treated with ranibizumab
por: Oh, Ha Na, et al.
Publicado: (2012)

Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report
por: Scalzo, Giovanna Carnovale, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_eq502h8jr3m6lt3rqgggbln588