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

[Congenital cranial dysinnervation disorders (CCDD)].

Klinische Monatsblatter fur Augenheilkunde - 1 Mar 2015

Nentwich M M, Nentwich M F, Maertz J, Brandlhuber U, Rudolph G

Abstract excerpt

Knowledge about hereditary eye diseases has been substantially increased by means of genetic testing during the last decade. This has resulted in a new classification of a number of disease patterns, which are characterised by non-progressive restrictive disorders of the oculomotor system, formerly classified as "congenital fibrosis syndromes". Based on the results of genetic testing, these ocular motility...

Read the complete abstract on PubMed

Topics

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

Share to Eye Diseases, Hereditary
Share to Fibrosis
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Models, Genetic

Share to Molecular Diagnostic Techniques

Share to Ophthalmoplegia

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 25803556
DOI: 10.1055/s-0041-100772

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

[Congenital cranial dysinnervation disorders (CCDD)].PMID 25803556Read ↗

Congenital cranial dysinnervation disorders.Semantic proximity Read ↗

[Congenital fibrosis of extraocular muscles (CFEOM) and other phenotypes of congenital cranial dysinnervation syndromes (CCDD)].Semantic proximity Read ↗

Congenital Fibrosis of the Extraocular Muscles: An Overview from Genetics to ManagementSemantic proximity Read ↗

Congenital and Genetic Ocular Motility Disorders: Update and Considerations.Semantic proximity Read ↗

Recent progress in understanding congenital cranial dysinnervation disorders.Semantic proximity Read ↗

Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.Semantic proximity Read ↗

Congenital fibrosis of the extra-ocular muscles (CFEOM) and the cranial dysinnervation disorders.Semantic proximity Read ↗

The Genetic Basis of Incomitant Strabismus: Consolidation of the Current Knowledge of the Genetic Foundations of DiseaseSemantic proximity Read ↗

Oculomotility Disorders Arising From Disruptions in Brainstem Motor Neuron DevelopmentSemantic proximity Read ↗

Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.Semantic proximity Read ↗

The congenital cranial dysinnervation disorders.Semantic proximity Read ↗

Congenital Cranial Dysinnervation Disorders: A Literature Review.Semantic proximity Read ↗

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