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

Nanophthalmos: A Review of the Clinical Spectrum and Genetics

1 Jan 2018

Abstract excerpt

Nanophthalmos is a clinical spectrum of disorders with a phenotypically small but structurally normal eye. These disorders present significant clinical challenges to ophthalmologists due to a high rate of secondary angle-closure glaucoma, spontaneous choroidal effusions, and perioperative complications with cataract and retinal surgeries. Nanophthalmos may present as a sporadic or familial disorder, with...

Read the complete abstract on PubMed

Topics

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

Share to Corneal Surgery and Treatments
Share to Ocular Diseases and Behçet’s Syndrome
Share to Ocular Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29862063
DOI: 10.1155/2018/2735465

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nanophthalmos: A Review of the Clinical Spectrum and GeneticsPMID 29862063Read ↗

The genetic and clinical landscape of nanophthalmos in an Australian cohortSemantic proximity Read ↗

The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohortSemantic proximity Read ↗

Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort.Semantic proximity Read ↗

Genotype-phenotype spectrum in isolated and syndromic nanophthalmos.Semantic proximity Read ↗

MFRP, PRSS56, and MYRF account for 60.5% of a Chinese cohort with nanophthalmos.Semantic proximity Read ↗

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56.Semantic proximity Read ↗

Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseSemantic proximity Read ↗

Clinical features of patients with mutations in genes for nanophthalmos.Semantic proximity Read ↗

Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse.Semantic proximity Read ↗

Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos.Semantic proximity Read ↗

Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic DisordersSemantic proximity Read ↗

Novel mutations in MFRP and PRSS56 are associated with posterior microphthalmos.Semantic proximity Read ↗

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