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Volumn 33, Issue 5, 1996, Pages 419-421

Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): A new syndrome

Author keywords

Ataxia; Deafness; Optic atrophy

Indexed keywords

ADULT; AREFLEXIA; ARTICLE; CASE REPORT; CEREBELLAR ATAXIA; FAMILIAL DISEASE; FEMALE; HUMAN; MALE; NEUROLOGIC DISEASE; OPTIC NERVE ATROPHY; PATHOPHYSIOLOGY; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDROME;

EID: 0029870946     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.5.419     Document Type: Article
Times cited : (55)

References (13)
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  • 2
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  • 3
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    • Familial ataxia, deaf mutism and muscular wasting
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    • X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course
    • Arts WFM, Loonen RCA, Sengers A, Slooff JL. X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course. Ann Neurol 1993;33:535-9.
    • (1993) Ann Neurol , vol.33 , pp. 535-539
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  • 6
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    • Matthews WB, Rundle AT. Familial cerebellar ataxia and hypogonadism. Brain 1964;87:463-8.
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    • Matthews, W.B.1    Rundle, A.T.2
  • 7
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    • Some unusual findings in a family with Friedreich's ataxia
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  • 10
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    • Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19pl3
    • Teh BT, Silburn P, Lindblad K, et al. Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19pl3. Am J Hum Genet 1995;56:1443-9.
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  • 11
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    • Optic atrophy, neural deafness and distal neurogenic amyotrophy. Report of a family with two affected siblings
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    • Iwashita, H.1    Inoue, N.2    Araki, S.3    Kuroiwa, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.