Challenging Diagnosis of Stickler Syndrome in a Patient with Premature Osteoarthritis: A Case Report
UMass Chan Affiliations
Department of Orthopedics and Physical RehabilitationDocument Type
Journal ArticlePublication Date
2021-03-23Keywords
hereditary progressive arthro-ophthalmopathyhip dysplasia
knee epiphyseal dysplasia
early-onset osteoarthritis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Diagnosis
Musculoskeletal Diseases
Orthopedics
Metadata
Show full item recordAbstract
CASE: A 53-year-old male patient, subsequently diagnosed with type I Stickler syndrome, presented with severe premature osteoarthritis associated with bilateral hip dysplasia and knee epiphyseal dysplasia. Despite the presence of the typical manifestations of orofacial defects, hearing, ocular, and musculoskeletal abnormalities, the patient had never been diagnosed with the syndrome. CONCLUSION: Stickler syndrome can present with a wide spectrum of musculoskeletal abnormalities without previous diagnosis. It is often underrecognized if the manifestations of other systems are not appreciated. Stickler syndrome should be considered in the differential diagnosis of patients with unexplained musculoskeletal abnormality particularly in the presence of other system manifestations.Source
Yousef MA, Ayers DC. Challenging Diagnosis of Stickler Syndrome in a Patient with Premature Osteoarthritis: A Case Report. JBJS Case Connect. 2021 Mar 23;11(1). doi: 10.2106/JBJS.CC.20.00687. PMID: 33755637. Link to article on publisher's site
DOI
10.2106/JBJS.CC.20.00687Permanent Link to this Item
http://hdl.handle.net/20.500.14038/29765PubMed ID
33755637Related Resources
ae974a485f413a2113503eed53cd6c53
10.2106/JBJS.CC.20.00687