Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene.

Ophthalmic genetics - 1 Dec 2016

Lai Yu-Hung, Capasso Jenina E, Kaiser Richard, Levin Alex V

Abstract excerpt

BACKGROUND: Cystoid macular edema (CME) and non-leaking intraretinal cystoid spaces (ICS) have different pathophysiologic mechanisms. MATERIALS AND METHODS: We report a patient with retinitis pigmentosa (RP) with ICS due to a mutation in the male germ cell-associated kinase (MAK) gene. RESULTS: A 41-year-old Ashkenazi Jewish male was referred for abnormal visual field revealed by regular optometric examination....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fluorescein Angiography
Share to Photoreceptor Cells, Vertebrate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Serine-Threonine Kinases

Share to Retinitis Pigmentosa

Share to Tomography, Optical Coherence

Share to Vision Disorders

Share to Visual Acuity

Share to Visual Fields

Source

Identifiers

PMID: 26894652
DOI: 10.3109/13816810.2015.1092046

Genes

MAK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene.PMID 26894652Read ↗

Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features.Semantic proximity Read ↗

Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.Semantic proximity Read ↗

Slowly progressive retinitis pigmentosa caused by two novel mutations in the MAK gene.Semantic proximity Read ↗

Negative regulation of ciliary length by ciliary male germ cell-associated kinase (Mak) is required for retinal photoreceptor survivalSemantic proximity Read ↗

Male germ cell-associated kinase (MAK) is required for axoneme formation during ciliogenesis in zebrafish photoreceptorsSemantic proximity Read ↗

Male germ cell-associated kinase is required for axoneme formation during ciliogenesis in zebrafish photoreceptors.Semantic proximity Read ↗

Five-Year Structural Progression in Monozygotic Twins with MAK Exon 3- Related Retinitis PigmentosaSemantic proximity Read ↗

Mevalonate kinase deficiency associated with ataxia and retinitis pigmentosa in two brothers with MVK gene mutations.Semantic proximity Read ↗

Ccrk-Mak/Ick kinase signaling axis is a ciliary transport regulator essential for retinal photoreceptor maintenanceSemantic proximity Read ↗

High-resolution Imaging in Male Germ Cell-Associated Kinase (MAK)-related Retinal Degeneration.Semantic proximity Read ↗

Cystoid Macular Edema in Non-Syndromic Retinitis Pigmentosa: Associations With Causative Genes in a Large Cohort.Semantic proximity Read ↗

Using Patient iPSC-derived Retinal Pigment Epithelial Cells to Evaluate Differential Susceptibility to MEK Inhibitor-Associated RetinopathySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.