Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter

Ted M. Burns; H. R. Jones; L. H. Phillips; T. L. Bugawan; H. A. Erlich; V. A. Lennon

doi:10.1212/01.WNL.0000092016.98256.21

Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter

Ted M. Burns, H. R. Jones, L. H. Phillips, T. L. Bugawan, H. A. Erlich, V. A. Lennon

Laboratory Medicine and Pathology

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

17 Scopus citations

Abstract

Stiff-person syndrome (SPS) is a sporadic autoimmune disorder characterized by muscle stiffness with painful spasms and usually a high level of GAD65 antibody. The authors report familial SPS associated with GAD65 antibody. The clinical presentations were disparate; the father had an appendicular form of SPS and the daughter's axial SPS presented with episodic opisthotonos.

Original language	English (US)
Pages (from-to)	1291-1293
Number of pages	3
Journal	Neurology
Volume	61
Issue number	9
DOIs	https://doi.org/10.1212/01.WNL.0000092016.98256.21
State	Published - Nov 11 2003

ASJC Scopus subject areas

Clinical Neurology

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10.1212/01.WNL.0000092016.98256.21

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abstract = "Stiff-person syndrome (SPS) is a sporadic autoimmune disorder characterized by muscle stiffness with painful spasms and usually a high level of GAD65 antibody. The authors report familial SPS associated with GAD65 antibody. The clinical presentations were disparate; the father had an appendicular form of SPS and the daughter's axial SPS presented with episodic opisthotonos.",

author = "Burns, {Ted M.} and Jones, {H. R.} and Phillips, {L. H.} and Bugawan, {T. L.} and Erlich, {H. A.} and Lennon, {V. A.}",

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AU - Burns, Ted M.

AU - Jones, H. R.

AU - Phillips, L. H.

AU - Bugawan, T. L.

AU - Erlich, H. A.

AU - Lennon, V. A.

PY - 2003/11/11

Y1 - 2003/11/11

N2 - Stiff-person syndrome (SPS) is a sporadic autoimmune disorder characterized by muscle stiffness with painful spasms and usually a high level of GAD65 antibody. The authors report familial SPS associated with GAD65 antibody. The clinical presentations were disparate; the father had an appendicular form of SPS and the daughter's axial SPS presented with episodic opisthotonos.

AB - Stiff-person syndrome (SPS) is a sporadic autoimmune disorder characterized by muscle stiffness with painful spasms and usually a high level of GAD65 antibody. The authors report familial SPS associated with GAD65 antibody. The clinical presentations were disparate; the father had an appendicular form of SPS and the daughter's axial SPS presented with episodic opisthotonos.

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ER -

Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter

Abstract

ASJC Scopus subject areas

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