Autosomal dominant cerebral arteriopathy: Neuropsychiatric syndrome in a family

Neuropsychiatry, Neuropsychology and Behavioral Neurology

Volumn 11, Issue 1, 1998, Pages 31-39

  Adair, John C ^a,b   Hart, Blaine L ^b   Kornfeld, Mario ^b   Graham, Glenn D ^a,b   Swanda, Rex M ^a   Ptacek, Louis J ^c   Davis, Larry E ^a,b  

^a VA Medical Center   (United States)

^b UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

CADASIL; Familial dementia; Hereditary dementia

Indexed keywords

ADULT; ARTERIOLE; ARTERY DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN BIOPSY; CASE REPORT; CLINICAL FEATURE; DEGENERATIVE DISEASE; DEMENTIA; FAMILIAL DISEASE; FATHER; FEMALE; HISTOPATHOLOGY; HUMAN; INTELLECT; LEUKOENCEPHALOPATHY; MALE; MENTAL DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PERSONALITY; PHENOTYPE; PRIORITY JOURNAL; SCLEROSIS; SIBLING; STROKE; WHITE MATTER;

ADULT; AGE OF ONSET; BRAIN; CEREBRAL ARTERIAL DISEASES; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; DEMENTIA, MULTI-INFARCT; DISEASE PROGRESSION; FEMALE; GENES, DOMINANT; HUMANS; LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL; MALE; MIDDLE AGED; NEUROPSYCHOLOGICAL TESTS; PEDIGREE; PHENOTYPE;

EID: 0031898673     PISSN: 0894878X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. Coker SB. The diagnosis of childhood neurodegenerative disorders presenting as dementia in adults. Neurology 1991;41:794-8.
2. Reichmann WE, Cummings JL. Diagnosis of rare dementia syndromes: an algorithmic approach. J Geriatr Psychiatry Neurol 1990;3:73-84.
3. Tournier-Lasserve E, Iba-Zizen MT, Romero N, Bousser MG. Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy. Stroke 1991;22:1297-1302.
4. Bannister R, ed. Autonomic Failure. NY: Oxford University Press, 1983.
5. Graham GD, Blamire AM, Howseman AM, et al. Proton magnetic resonance spectroscopy of cerebral lactate and other metabolites in stroke patients. Stroke 1992;23:333-40.
6. Castillo M, Kwock L, Green C. MELAS syndrome: imaging and proton MR spectroscopic findings. Am J Neuroradiol 1995;16:233-9.
7. Mitsias P, Levine SR. Cerebrovascular complications of Fabry's disease. Ann Neurol 1996;40:8-17.
8. Rebollo M, Val JF, Garijo F, Quintana F, Berciano J. Livedo reticularis and cerebrovascular lesions (Sneddon's syndrome). Brain 1983;106:965-79.
9. Babikian V, Ropper AH. Binswanger's disease: a review. Stroke 1987;18:2-12.
10. Roman GC. Senile dementia of the Binswanger type. JAMA 1987; 258:1782-8.
11. Bennett DA, Wilson RS, Gilley DW, Fox JH. Clinical diagnosis of Binswanger's disease. J Neurol Neurosurg Psychiatry 1990;53:961-5.
12. Lowenberg K, Hill TS. Diffuse sclerosis with preserved myelin islands. Arch Neurol Psychiatry 1933;29:1233-45.
13. Shapiro EG, Lockman LA, Knopman D, Krivit W. Characteristics of the dementia in late-onset metachromatic leukodystrophy. Neurology 1994;44:662-5.
14. Knopman D, Sung JH, Davis D. Progressive familial leukodystrophy of late onset. Neurology 1996;46:429-34.
15. Constantinidis J, Wisniewski TM. The dominant form of the pigmentary orthochromatic leukodystrophy. Acta Neuropathol (Berl) 1991;82:483-7.
16. Crome L, Hanefeld F, Patrick D, et al. Late onset globoid cell leucodystrophy. Brain 1973;96:841-8.
17. Bird TD, Koerker RM, Leaird BJ, Vlcek BW, Thorning DR. Lipomembranous polycystic osterodysplasia (brain, bone, and fat disease): a genetic cause of presenile dementia. Neurology 1983;33:81-6.
18. Walls TJ, Jones RA, Cartlidge NEF, Saunders M. Alexander's disease with rosenthal fibre formation in an adult. J Neurol Neurosurg Psychiatry 1984;47;399-403.
19. Eldridge R, Anayiotos CP, Schlesinger S, et al. Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis. N Engl J Med 1984;311:948-53.
20. Schwankhaus JD, Patronas N, Dorwart R, Eldridge R, Schlesinger S, McFarland H. Computed tomography and magnetic resonance imaging in adult-onset leukodystrophy. Arch Neurol 1988;45:1004-8.
21. Schwankhaus JD, Katz DA, Eldridge R, Schlesinger S, McFarland H. Clinical and pathological features of an autosomal dominant, adult-onset leukodystrophy simulating chronic progressive multiple sclerosis. Arch Neurol 1994;51:757-66.
22. Brown RT, Polinsky RJ, Schwankhaus J. et al. Adrenergic dysfunction in hereditary adult-onset leukodystrophy. Neurology 1987;37:1421-4.
23. Lanska DJ, Currier RD, Cohen M, et al. Familial progressive subcortical gliosis. Neurology 1994;44:1633-43.
24. Neumann MA, Cohn R. Progressive subcortical gliosis, a rare form of pre-senile dementia. Brain 1967;90:405-27.
25. Bousser MG, Tournier-Lasserve E. Summary of the proceedings of the first international workshop on CADASIL. Stroke 1994;25:704-7.
26. Chabriat H, Vahedi K, Iba-Zizen MT, et al. Clinical spectrum of CADASIL: a study of 7 families. Lancet 1995;346:934-9.
27. Ragno M, Tournier-Lasserve E, Fiori MG, et al. An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Ann Neurology 1995;38:231-6.
28. Mas JL, Diouya A, De Recondo J. A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy. Neurology 1992;42:1015-9.
29. Hutchinson M, O'Riordan J, Javed M, et al. Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann Neurol 1995;38:817-24.
30. Skehan SJ, Hutchinson M, MacErlaine DP. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR findings. Am J Neuroradiol 1995;16:2115-9.
31. Tournier-Lasserve E, Jourtel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet 1993;3:256-9.
32. Baudrimont M, Dubas F, Joutel A, Tournier-Lasserve E, Bousser MG. Autosomal dominant leukoencephalopathy and subcortical stroke: A clinicopathologic study. Stroke 1993;24:122-5.
33. Zhang WW, Ma KC, Andersen O, Sourander P, Tollesson PO, Olsson Y. The microvascular changes in cases of hereditary multiinfarct disease of the brain. Acta Neuropathol 1994;87:317-24.
34. Lammie GA, Rakshi J, Rossor MN, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)-confirmation by cerebral biopsy in 2 cases. Clin Neuropath 1995;14:201-6.
35. Sabbadini G, Francia A, Calandriello L, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): clinical, neuroimaging, pathological and genetic study of a large Italian family. Brain 1995;118:207-15.
36. Ruchoux MM, Guerouaou D, Vandenhaute B, et al. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Acta Neuropath 1995;89:500-12.
37. Bowler JV, Hachinski V. Progress in the genetics of cerebrovascular disease: inherited subcortical arteriopathies. Stroke 1994; 25:1696-8.
38. Malandrini A, Carrera P, Ciacci G, et al. Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy. Neurology 1997;48:1200-3.