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

Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.

American journal of medical genetics. Part C, Seminars in medical genetics - 1 Mar 2015

Castori Marco, Dordoni Chiara, Morlino Silvia, Sperduti Isabella, Ritelli Marco, Valiante Michele, Chiarelli Nicola, Zanca Arianna, Celletti Claudia, Venturini Marina, Camerota Filippo, Calzavara-Pinton Piergiacomo, Grammatico Paola, Colombi Marina

Abstract excerpt

Cutaneous manifestations are a diagnostic criterion of Ehlers-Danlos syndrome, hypermobility type (EDS-HT) and joint hypermobility syndrome (JHS). These two conditions, originally considered different disorders, are now accepted as clinically indistinguishable and often segregate as a single-fami...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Atrophy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Cicatrix

Share to Ehlers-Danlos Syndrome

Share to Joint Instability

Share to Skin Abnormalities

Source

Identifiers

PMID: 25655071
DOI: 10.1002/ajmg.c.31425

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25655071-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.PMID 25655071Read ↗

Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type.Semantic proximity Read ↗

Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type: a study of intrafamilial and interfamilial variability in 23 Italian pedigrees.Semantic proximity Read ↗

Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives.Semantic proximity Read ↗

Natural history and manifestations of the hypermobility type Ehlers-Danlos syndrome: a pilot study on 21 patients.Semantic proximity Read ↗

Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients.Semantic proximity Read ↗

Placing joint hypermobility in context: traits, disorders and syndromes.Semantic proximity Read ↗

The Many Facets of Hypermobile Ehlers-Danlos SyndromeSemantic proximity Read ↗

Ehlers-Danlos syndrome: recent advances and current understanding of the clinical and genetic heterogeneity.Semantic proximity Read ↗

Transcriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type.Semantic proximity Read ↗

Defining Neuro-EDS: A Neuro-Predominant Phenotype in hEDS/HSD and Related Heritable Connective Tissue DisordersSemantic proximity Read ↗

Bridging the Diagnostic Gap for Hypermobile Ehlers‐Danlos Syndrome and Hypermobility Spectrum Disorders: Evidence of a Common Extracellular Matrix Fragmentation Pattern in Patient Plasma as a Potential BiomarkerSemantic proximity Read ↗

Contemporary approach to joint hypermobility and related disorders.Semantic proximity Read ↗

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