Ehlers–Danlos syndrome (hypothesized)

E470862

Ehlers–Danlos syndrome (hypothesized) refers to a proposed diagnosis suggesting that the famed violinist Niccolò Paganini may have had a hereditary connective tissue disorder characterized by joint hypermobility, skin elasticity, and tissue fragility.

Try in SPARQL Jump to: Statements Referenced by

Statements (30)

Predicate Object
instanceOf medical hypothesis
proposed medical diagnosis
appliesTo Niccolò Paganini NERFINISHED
associatedWith hereditary connective tissue disorders
basedOn accounts of Niccolò Paganini’s unusual physical appearance
historical descriptions of Niccolò Paganini’s physical features
reports of extreme flexibility in Niccolò Paganini’s fingers and joints
characterizedBy joint hypermobility
skin hyperextensibility
tissue fragility
concerns possible genetic basis for Niccolò Paganini’s physical traits
describes a hereditary connective tissue disorder
distinctFrom clinically diagnosed Ehlers–Danlos syndrome
hasEvidenceType biographical reports
indirect historical evidence
hasUncertainStatus not clinically confirmed
retrospective diagnosis
notSupportedBy contemporary clinical examination records confirming EDS
direct genetic testing of Niccolò Paganini
refersTo a proposed diagnosis for Niccolò Paganini
relatedConcept retrospective diagnosis of historical figures
relatedTo Ehlers–Danlos syndromes NERFINISHED
subjectOf speculation in medical literature
speculation in musicological literature
suggestedBy some medical historians
some physicians
timeOfFormulation 20th–21st century medical literature
usedToExplain Niccolò Paganini’s extreme finger span
Niccolò Paganini’s joint laxity
Niccolò Paganini’s reported skin and tissue fragility

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

Niccolò Paganini medicalCondition Ehlers–Danlos syndrome (hypothesized)