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

Co-morbidity of Emery-Dreifuss muscular dystrophy and a congenital myasthenic syndrome possibly affecting the phenotype in a large Bedouin kindred.

European journal of neurology - 1 Mar 2007

Ifergane G, Al-Sayed I, Birk O, Harel T, Wirguin I

Abstract excerpt

Emery-Dreifuss muscular dystrophy (EDMD) is an X-linked humero-peroneal muscular dystrophy associated with contractures and cardiomyopathy. In a 90 member family, we found 11 affected male individuals, three of whom displayed areflexia and neurogenic electromyographic changes. Muscle biopsy perfo...

Read the complete abstract on PubMed

Topics

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

Share to Arabs
Share to Comorbidity
Share to Disease Progression

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, X-Linked

Share to Genetic Linkage

Share to Muscle, Skeletal

Share to Muscular Dystrophy, Emery-Dreifuss

Share to Myasthenic Syndromes, Congenital

Source

Identifiers

PMID: 17355552
DOI: 10.1111/j.1468-1331.2006.01657.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17355552-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Co-morbidity of Emery-Dreifuss muscular dystrophy and a congenital myasthenic syndrome possibly affecting the phenotype in a large Bedouin kindred.PMID 17355552Read ↗

Emery dreifuss muscular dystrophy: a clinico-pathological study.Semantic proximity Read ↗

Emery-Dreifuss muscular dystrophy.Semantic proximity Read ↗

Emery-Dreifuss muscular dystrophy.Semantic proximity Read ↗

Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy.Semantic proximity Read ↗

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.Semantic proximity Read ↗

Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy.Semantic proximity Read ↗

Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype.Semantic proximity Read ↗

Limb-girdle muscular dystrophy due to emerin gene mutations.Semantic proximity Read ↗

Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression.Semantic proximity Read ↗

Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy.Semantic proximity Read ↗

X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort study.Semantic proximity Read ↗

Identification of novel mutations in three families with Emery-Dreifuss muscular dystrophy.Semantic proximity Read ↗

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