Unusual presentation of CADASIL with reversible coma and confusion

Neurology

Volumn 59, Issue 7, 2002, Pages 1115-1116

  Le Ber, I ^a   Carluer, L ^a   Derache, N ^a   Lalevee C ^a   Ledoze, F ^a   Defer, Gilles Louis ^a  

^a CHU CÔTE DE NACRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; AUTOSOMAL DISORDER; CADASIL; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; COMA; CONFUSION; DISEASE COURSE; FEMALE; HUMAN; LABORATORY TEST; NEUROLOGIC EXAMINATION; NEUROPSYCHOLOGICAL TEST; NOTE; PRIORITY JOURNAL;

EID: 0037044266     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.59.7.1115     Document Type: Note

References (6)

1. Dichgans M, Mayer M, Uttner I, et al. The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol 1998;44:731-739.
2. Hutchinson M, O'Riordan J, Javed M, et al. Familial hemiplegic migraine and autosomal dominant arteriopathy.with leukoencephalopathy (CADASIL). Ann Neurol 1995;38:817-824.
3. Vérin M, Rolland Y, Landgraf F, et al. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent feature. J Neurol Neurosurg Psychiatry 1995;59:579-585.
4. Mellies JK, Bäumer T, Müller JA, et al. SPECT study of a German CADASIL family. A phenotype with migraine and progressive dementia only. Neurology 1998;50:1715-1721.
5. Ceroni M, Poloni TE, Tonietti S, et al. Migraine with aura and white matter abnormalities: Notch3 mutation. Neurology 2000;54:1869-1871.
6. Chabriat H, Tournier-Lasserve E, Vahedi K, et al. Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Neurology 1995;45:1086-1091.