Benign hereditary chorea

Patricia G. Wheeler; David D. Weaver; William B. Dobyns

doi:10.1016/0887-8994(93)90101-H

Benign hereditary chorea

Patricia G. Wheeler, David D. Weaver, William B. Dobyns

Pediatric Genetics & Metabolism

Research output: Contribution to journal › Review article › peer-review

19 Scopus citations

Abstract

Benign hereditary chorea is an uncommon inherited form of childhood chorea that can be mistaken for much more serious disorders, such as Huntington disease. The clinical manifestations of this condition are reviewed, emphasizing the differential diagnosis, treatment modalities, and evaluation of childhood chorea.

Original language	English (US)
Pages (from-to)	337-340
Number of pages	4
Journal	Pediatric Neurology
Volume	9
Issue number	5
DOIs	https://doi.org/10.1016/0887-8994(93)90101-H
State	Published - 1993

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title = "Benign hereditary chorea",

abstract = "Benign hereditary chorea is an uncommon inherited form of childhood chorea that can be mistaken for much more serious disorders, such as Huntington disease. The clinical manifestations of this condition are reviewed, emphasizing the differential diagnosis, treatment modalities, and evaluation of childhood chorea.",

author = "Wheeler, {Patricia G.} and Weaver, {David D.} and Dobyns, {William B.}",

year = "1993",

doi = "10.1016/0887-8994(93)90101-H",

language = "English (US)",

volume = "9",

pages = "337--340",

journal = "Pediatric Neurology",

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T1 - Benign hereditary chorea

AU - Wheeler, Patricia G.

AU - Weaver, David D.

AU - Dobyns, William B.

PY - 1993

Y1 - 1993

N2 - Benign hereditary chorea is an uncommon inherited form of childhood chorea that can be mistaken for much more serious disorders, such as Huntington disease. The clinical manifestations of this condition are reviewed, emphasizing the differential diagnosis, treatment modalities, and evaluation of childhood chorea.

AB - Benign hereditary chorea is an uncommon inherited form of childhood chorea that can be mistaken for much more serious disorders, such as Huntington disease. The clinical manifestations of this condition are reviewed, emphasizing the differential diagnosis, treatment modalities, and evaluation of childhood chorea.

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U2 - 10.1016/0887-8994(93)90101-H

DO - 10.1016/0887-8994(93)90101-H

M3 - Review article

C2 - 8292207

AN - SCOPUS:0027429748

SN - 0887-8994

VL - 9

SP - 337

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JO - Pediatric Neurology

JF - Pediatric Neurology

IS - 5

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Benign hereditary chorea

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