Neuropathic sternoclavicular joint secondary to syringomyelia: A case report

L. K. Chidgey; Robert M Szabo; D. R. Benson

Neuropathic sternoclavicular joint secondary to syringomyelia: A case report

L. K. Chidgey, Robert M Szabo, D. R. Benson

Orthopaedic Surgery

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

8 Scopus citations

Abstract

A 14-year-old boy is presented with a syringomyelia and a neuropathic sternoclavicular joint. Recognition of neuropathic arthropathy of the upper extremity is important when a massive, destructive joint lesion exists in a patient with syringomyelia.

Original language	English (US)
Pages (from-to)	1571-1573
Number of pages	3
Journal	Orthopedics
Volume	11
Issue number	11
State	Published - 1988

ASJC Scopus subject areas

Orthopedics and Sports Medicine
Surgery

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title = "Neuropathic sternoclavicular joint secondary to syringomyelia: A case report",

abstract = "A 14-year-old boy is presented with a syringomyelia and a neuropathic sternoclavicular joint. Recognition of neuropathic arthropathy of the upper extremity is important when a massive, destructive joint lesion exists in a patient with syringomyelia.",

author = "Chidgey, {L. K.} and Szabo, {Robert M} and Benson, {D. R.}",

year = "1988",

language = "English (US)",

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T2 - A case report

AU - Chidgey, L. K.

AU - Szabo, Robert M

AU - Benson, D. R.

PY - 1988

Y1 - 1988

N2 - A 14-year-old boy is presented with a syringomyelia and a neuropathic sternoclavicular joint. Recognition of neuropathic arthropathy of the upper extremity is important when a massive, destructive joint lesion exists in a patient with syringomyelia.

AB - A 14-year-old boy is presented with a syringomyelia and a neuropathic sternoclavicular joint. Recognition of neuropathic arthropathy of the upper extremity is important when a massive, destructive joint lesion exists in a patient with syringomyelia.

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M3 - Article

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AN - SCOPUS:0023716849

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JO - Orthopedics

JF - Orthopedics

SN - 0147-7447

IS - 11

ER -

Neuropathic sternoclavicular joint secondary to syringomyelia: A case report

Abstract

ASJC Scopus subject areas

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