Otospondylomegaepiphyseal Dysplasia

Benjamin R. Williams; Amy R.U.L. Calhoun; Kenneth J. Holton; Brandon J. Kelly; Jonathan N. Sembrano

doi:10.2106/JBJS.CC.20.00140

Otospondylomegaepiphyseal Dysplasia

Benjamin R. Williams, Amy R.U.L. Calhoun, Kenneth J. Holton, Brandon J. Kelly, Jonathan N. Sembrano

Orthopaedic Surgery

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Case:We present a long-term follow-up on a woman with otospondylomegaepiphyseal dysplasia (OSMED). At the age of 46 years, she is one of the oldest patients with the syndrome in the literature to date. We focus on the musculoskeletal anatomy and orthopaedic interventions over her lifetime.Conclusion:OSMED is a very rare syndrome. Arthritis and joint pains presented in her early adolescence and progressed to the point of requiring joint replacements by her 20s. Early intervention and monitoring improved the quality of life for this patient.

Original language	English (US)
Pages (from-to)	E20.00140
Journal	JBJS case connector
Volume	10
Issue number	4
DOIs	https://doi.org/10.2106/JBJS.CC.20.00140
State	Published - Oct 16 2020

Bibliographical note

Publisher Copyright:
© 2020 Lippincott Williams and Wilkins. All rights reserved.

Access

10.2106/JBJS.CC.20.00140

OpenUrl availability

Full text

Cite this

@article{80b99b1f4e6345b88e3f710c676b0b84,

title = "Otospondylomegaepiphyseal Dysplasia",

abstract = "Case:We present a long-term follow-up on a woman with otospondylomegaepiphyseal dysplasia (OSMED). At the age of 46 years, she is one of the oldest patients with the syndrome in the literature to date. We focus on the musculoskeletal anatomy and orthopaedic interventions over her lifetime.Conclusion:OSMED is a very rare syndrome. Arthritis and joint pains presented in her early adolescence and progressed to the point of requiring joint replacements by her 20s. Early intervention and monitoring improved the quality of life for this patient.",

author = "Williams, {Benjamin R.} and Calhoun, {Amy R.U.L.} and Holton, {Kenneth J.} and Kelly, {Brandon J.} and Sembrano, {Jonathan N.}",

year = "2020",

month = oct,

day = "16",

doi = "10.2106/JBJS.CC.20.00140",

language = "English (US)",

volume = "10",

pages = "E20.00140",

journal = "JBJS case connector",

issn = "2160-3251",

publisher = "Lippincott Williams and Wilkins",

number = "4",

}

TY - JOUR

T1 - Otospondylomegaepiphyseal Dysplasia

AU - Williams, Benjamin R.

AU - Calhoun, Amy R.U.L.

AU - Holton, Kenneth J.

AU - Kelly, Brandon J.

AU - Sembrano, Jonathan N.

PY - 2020/10/16

Y1 - 2020/10/16

N2 - Case:We present a long-term follow-up on a woman with otospondylomegaepiphyseal dysplasia (OSMED). At the age of 46 years, she is one of the oldest patients with the syndrome in the literature to date. We focus on the musculoskeletal anatomy and orthopaedic interventions over her lifetime.Conclusion:OSMED is a very rare syndrome. Arthritis and joint pains presented in her early adolescence and progressed to the point of requiring joint replacements by her 20s. Early intervention and monitoring improved the quality of life for this patient.

AB - Case:We present a long-term follow-up on a woman with otospondylomegaepiphyseal dysplasia (OSMED). At the age of 46 years, she is one of the oldest patients with the syndrome in the literature to date. We focus on the musculoskeletal anatomy and orthopaedic interventions over her lifetime.Conclusion:OSMED is a very rare syndrome. Arthritis and joint pains presented in her early adolescence and progressed to the point of requiring joint replacements by her 20s. Early intervention and monitoring improved the quality of life for this patient.

UR - http://www.scopus.com/inward/record.url?scp=85100609883&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85100609883&partnerID=8YFLogxK

U2 - 10.2106/JBJS.CC.20.00140

DO - 10.2106/JBJS.CC.20.00140

M3 - Article

C2 - 33512935

AN - SCOPUS:85100609883

SN - 2160-3251

VL - 10

SP - E20.00140

JO - JBJS case connector

JF - JBJS case connector

IS - 4

ER -

Otospondylomegaepiphyseal Dysplasia

Abstract

Bibliographical note

Access

OpenUrl availability

Other files and links

Fingerprint

Cite this