Partial NADH dehydrogenase defect presenting as spastic cerebral palsy

Chang Y. Tsao; Francis S. Wright; Carl P. Boesel; Mark Luquette

doi:10.1016/0387-7604(94)90127-9

Partial NADH dehydrogenase defect presenting as spastic cerebral palsy

Chang Y. Tsao, Francis S. Wright, Carl P. Boesel, Mark Luquette

Laboratory Medicine and Pathology

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

6 Scopus citations

Abstract

Mitochondrial myopathies are heterogeneous disorders. They may present at any age with a variable clinical course. We report a 6-year-old boy presenting as spastic cerebral palsy for 4 years, then athetotic movements and loss of milestones. He was eventually found to have NADH dehydrogenase deficiency.

Original language	English (US)
Pages (from-to)	393-395
Number of pages	3
Journal	Brain and Development
Volume	16
Issue number	5
DOIs	https://doi.org/10.1016/0387-7604(94)90127-9
State	Published - 1994

Keywords

Athetotic movement
Mitochondrial myopathy
NADH dehydrogenase deficiency
Spastic cerebral palsy

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10.1016/0387-7604(94)90127-9

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@article{9f9c4ac9eb60492fa1c5b338235d5773,

title = "Partial NADH dehydrogenase defect presenting as spastic cerebral palsy",

abstract = "Mitochondrial myopathies are heterogeneous disorders. They may present at any age with a variable clinical course. We report a 6-year-old boy presenting as spastic cerebral palsy for 4 years, then athetotic movements and loss of milestones. He was eventually found to have NADH dehydrogenase deficiency.",

keywords = "Athetotic movement, Mitochondrial myopathy, NADH dehydrogenase deficiency, Spastic cerebral palsy",

author = "Tsao, {Chang Y.} and Wright, {Francis S.} and Boesel, {Carl P.} and Mark Luquette",

year = "1994",

doi = "10.1016/0387-7604(94)90127-9",

language = "English (US)",

volume = "16",

pages = "393--395",

journal = "Brain and Development",

issn = "0387-7604",

publisher = "Elsevier B.V.",

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}

TY - JOUR

T1 - Partial NADH dehydrogenase defect presenting as spastic cerebral palsy

AU - Tsao, Chang Y.

AU - Wright, Francis S.

AU - Boesel, Carl P.

AU - Luquette, Mark

PY - 1994

Y1 - 1994

N2 - Mitochondrial myopathies are heterogeneous disorders. They may present at any age with a variable clinical course. We report a 6-year-old boy presenting as spastic cerebral palsy for 4 years, then athetotic movements and loss of milestones. He was eventually found to have NADH dehydrogenase deficiency.

AB - Mitochondrial myopathies are heterogeneous disorders. They may present at any age with a variable clinical course. We report a 6-year-old boy presenting as spastic cerebral palsy for 4 years, then athetotic movements and loss of milestones. He was eventually found to have NADH dehydrogenase deficiency.

KW - Athetotic movement

KW - Mitochondrial myopathy

KW - NADH dehydrogenase deficiency

KW - Spastic cerebral palsy

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UR - http://www.scopus.com/inward/citedby.url?scp=0027949132&partnerID=8YFLogxK

U2 - 10.1016/0387-7604(94)90127-9

DO - 10.1016/0387-7604(94)90127-9

M3 - Article

C2 - 7892959

AN - SCOPUS:0027949132

SN - 0387-7604

VL - 16

SP - 393

EP - 395

JO - Brain and Development

JF - Brain and Development

IS - 5

ER -

Partial NADH dehydrogenase defect presenting as spastic cerebral palsy

Abstract

Keywords

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