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

Coats-like retinopathy in an infant with preclinical facioscapulohumeral dystrophy.

Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus - 1 Apr 2012

Ganesh Anuradha, Kaliki Swathi, Shields Carol L

Abstract excerpt

Facioscapulohumeral dystrophy (FSHD) is an autosomal-dominant disorder characterized by weakness of the face, upper arm, shoulder, and lower limb musculature, with an onset between the first and third decades. Coats disease is a congenital disorder of retinal vascular development characterized by unilateral peripheral retinal telangiectasia and progressive subretinal and intraretinal exudation. This condition has...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 4
Share to Fluorescein Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Muscular Dystrophy, Facioscapulohumeral

Share to Mutation

Share to Retinal Vessels

Share to Tomography, Optical Coherence

Share to Visual Acuity

Source

Identifiers

PMID: 22525183
DOI: 10.1016/j.jaapos.2011.11.005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Coats-like retinopathy in an infant with preclinical facioscapulohumeral dystrophy.PMID 22525183Read ↗

Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa.Semantic proximity Read ↗

Phenotype of Coats disease in females.Semantic proximity Read ↗

High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

A case of CRB1-negative Coats-like retinitis pigmentosa.Semantic proximity Read ↗

Coat's like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options.Semantic proximity Read ↗

[Extensive yellowish fundus changes in a 6-year-old child].Semantic proximity Read ↗

Radial perivascular retinal degeneration: a key to the clinical diagnosis of an ocular variant of Stickler syndrome with minimal or no systemic manifestations.Semantic proximity Read ↗

Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) or "Coats Plus": when peripheral retinal vasculature signals neurologic disease.Semantic proximity Read ↗

A Case of Bilateral Posner-Schlossman Syndrome in a Child with Familial Exudative VitreoretinopathySemantic proximity Read ↗

Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome.Semantic proximity Read ↗

Retinal findings and a novel TINF2 mutation in Revesz syndrome: Clinical and molecular correlations with pediatric retinal vasculopathies.Semantic proximity Read ↗

Retinal Dystrophy, Obesity and Hypertension in an Adolescent BoySemantic proximity Read ↗

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