Genetics of intracranial aneurysms

Neurosurgery

Volumn 40, Issue 4, 1997, Pages 651-663

  Schievink, Wouter I ^a  

^a MAYO CLINIC   (United States)

Author keywords

Cerebral aneurysym; Familial; Genetics; Screening; Subarachnoid hemorrhage

Indexed keywords

ANEURYSM RUPTURE; EHLERS DANLOS SYNDROME; GENETIC PREDISPOSITION; GENETIC SCREENING; HUMAN; INHERITANCE; INTRACRANIAL ANEURYSM; KIDNEY POLYCYSTIC DISEASE; MARFAN SYNDROME; NEUROFIBROMATOSIS; PRIORITY JOURNAL; REVIEW; SUBARACHNOID HEMORRHAGE;

CONNECTIVE TISSUE DISEASES; DISEASES IN TWINS; EHLERS-DANLOS SYNDROME; GENETIC HETEROGENEITY; GENETIC SCREENING; HUMANS; INTRACRANIAL ANEURYSM; MARFAN SYNDROME; NEUROFIBROMATOSIS 1; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; SUBARACHNOID HEMORRHAGE;

EID: 0030941167     PISSN: 0148396X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006123-199704000-00001     Document Type: Review

References (120)

1. Andrews RJ: Intracranial aneurysms: Characteristics of aneurysms in siblings. N Engl J Med 297:115, 1977 (letter).
2. Aoyama T, Francke U, Gasner C, Furthmayr H: Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders. Am J Med Genet 58:169-176, 1995.
3. Ashley CT, Warren ST: Trinucleotide repeat expansion and human disease. Annu Rev Genet 29:703-728, 1995.
4. Atkinson JLD, Sundt TM Jr, Houser OW, Whisnant JP: Angiographie frequency of anterior circulation intracranial aneurysms. J Neurosurg 70:551-555, 1989.
5. Austin GM, Schievink W, Williams R: Controlled pressurevolume factors in the enlargement of intracranial aneurysms. Neurosurgery 24:722-730, 1989.
6. Bailey 1C: Familial subarachnoid haemorrhage. Ulster Med J 62:119-126, 1993.
7. Beighton P: The Ehlers-Danlos syndromes, in Beighton P (ed): McKusick's Heritable Disorders of Connective Tissue. St Louis, Mosby, 1993, ed 5, pp 189-251.
8. Benatar MG: Intracranial fusiform aneurysms in von Recklinghausen's disease: Case report and literature review. J Neurol Neurosurg Psychiatry 57:1279-1280, 1994.
9. Black WC: Intracranial aneurysm in adult polycystic kidney disease: Is screening with MR angiography indicated? Radiology 191:18-20, 1994.
10. Borelius J: Zur Genese und klinischen Diagnose der polycystischen Degeneration der Nieren. Nord Med Ark 34:1-21, 1901.
11. Bromberg JEC, Rinkel GJE, Algra A, Greebe P, van Duyn CM, Kasan D, Limburg M, ter Berg HWM, Wijdicks EFM, van Gijn J: Subarachnoid haemorrhage in first- and second-degree relatives of patients with subarachnoid haemorrhage. Br Med J 311:288289, 1995.
12. Bromberg JEC, Rinkel GJE, Algra A, Limburg M, van Gijn J: Outcome in familial subarachnoid hemorrhage. Stroke 26:961963, 1995.
13. Bromberg JEC, Rinkel GJE, Algra A, van Duyn CM, Greebe P, Ramos LMP, van Gijn J: Familial subarachnoid hemorrhage: Distinctive features and patterns of inheritance. Ann Neurol 38:929-934, 1995.
14. Butler WE, Barker FG II, Crowell RM: Patients with polycystic kidney disease \vould benefit from routine magnetic resonance angiographie screening for intracerebral aneurysms: A decision analysis. Neurosurgery 38:506-516, 1996.
15. Byers PH: Ehlers-Danlos syndrome Type IV: A genetic disorder in many guises. J Invest Dermatol 105:311-313, 1995.
16. Chambers WR, Harper BF Jr, Simpson JR: Familial incidence of congenital aneurysms of cerebral arteries: Report of cases of ruptured aneurysms in father and son. JAMA 155:358-359,1954.
17. Chapman AB, Johnson AM, Gabow PA: Intracranial aneurysms in patients with autosomal dominant polycystic kidney disease: How to diagnose and who to screen. Am J Kidney Dis 22:526531, 1993.
18. Chapman AB, Rubinstein D, Hughes R, Stears JC, Earnest MP, Johnson AP, Gabow PA, Kaehny WD: Intracranial aneurysms in autosomal dominant polycystic kidney disease. N Engl J Med 327:916-920, 1992.
19. Chauveau D, Pirson Y, Verellen-Dumoulin C, Macnicol A, Gonzalo A, Gmnfcld JP: Intracranial aneurysms in autosomal dominant polycystic kidney disease. Kidney Int 45:1140-1146,1994.
20. Chauveau D, Sirieix M-E, Schillenger F, Legendre C, Grunfeld J-P: Recurrent rupture of intracranial aneurysms in autosomal dominant polycystic kidney disease. Br Mcd J 301:966-967,1990.
21. Crowell RM, Ogilvy CS, Gress DR: Unruptured aneurysms, in Ojemann RG, Ogilvy CS, Crowell RM, Heros RC (eds): Surgical Management of Neiirovasatlar Disease. Baltimore, Williams & Wilkins, 1995, ed 3, pp 205-222.
22. Daoust MC, Reynolds DM, Bichet DG, Somlo S: Evidence for a third genetic locus for autosomal dominant polycystic kidney disease. Genomics 25:733-736, 1995.
23. de Braekeleer M, Pérusse L, Cantin L, Bouchard J-M, Mathieu J: A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac-Saint-Jean region (Quebec, Canada). Ann Hum Genet 60:99-104, 1996.
24. de Wazières B, Coppere B, Durieu I, Fest T, Ninet J, Levrat R, Vuitton DA, Dupond JL: Manifestations vasculaires et/ou cardiaques du syndrome d'Ehlers-Danlos de Type IV: 9 observations. Presse Med 24:1381-1385, 1995.
25. Dietz HC, Pyeritz RE: Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders. Hum Mol Genet 4:1799-1809, 1995.
26. Falk A, Schmieder K, Hentsch A, Harders A, Heuser L: 3-DMT-TONE-Magnetresonanzangiographie zum Nachweis intrakranieller Aneurysmen im Vergleich zur digitalen Subtraktionsangiographie: Ein prospektive Studie. Fortschr Rontgenstr 164: 31-37, 1996.
27. Ferris NJ: MR angiographie screening for intracranial aneurysms: Is it worthwhile? Neuroradiology 37[Suppl 1: 544, 1995 (abstr).
28. Francke U, Berg MA, Tynan K, Brenn T, Liu W, Aoyama T, Gasner C, Miller DC, Furthmayr H: A Glyll27Ser mutation in an EGF-like domain of the fibrillin-l gene is a risk factor for ascending aortic aneurysm and dissection. Am J Hum Genet 56:12871296, 1995.
29. Fukawa O, Aihara H: Familial intracranial aneurysms: Report of 20 cases in eight families and review of the literature [in Japanese]. No Shinkei Geka 15:911-919, 1987.
30. Gabow PA: Autosomal dominant polycystic kidney disease. N Engl J Med 329:332-342, 1993.
31. Godfrey M: The Marfan syndrome, in Beighton P (ed): McKusick's Heritable Disorders of Connective Tissue. St Louis, Mosby, 1993, ed 5, pp 51-135.
32. Greene JF, Fitzwater JE, Burgess J: Arterial lesions associated with neurofibromatosis. Am J Clin Pathol 62:481-487, 1974.
33. Gregory PE, Gutmann DH, Mitchell A, Park J, Boguski M, Jacks T, Wood DL, Jove R, Collins FS: Neurofibromatosis Type 1 gene product (neurofibromin) associates with microtubules. Somat Cell Mol Genet 19:265-274, 1993.
34. Gutmann DH, Collins FS: The neurofibromatosis Type 1 gene and its protein product, neurofibromin. Neuron 10:335-343, 1993.
35. Harris PC, Ward CJ, Peral B, Hughes J: Autosomal dominant polycystic kidney disease: Molecular analysis. Hum Mol Genet 4:1745-1749, 1995.
36. Hashimoto I: Familial aneurysms and cerebral vascular anomalies. J Neurosurg 46:419-427, 1977.
37. Henkemeyer M, Rossi DJ, Holmyard DP, Puri MC, Mbamalu G, Harpal K, Shih TS, Jacks T, Pawson T: Vascular system defects and neuronal apoptosis in mice lacking RAS GTPase-activating protein. Nature 377:695-701, 1995.
38. Hope JKA, Wilson JL, Thomson FJ: Three-dimensional CT angiography in the detection and characterization of intracranial berry aneurysms. AJNR Am J Neuroradiol 17:439-445, 1996.
39. Hughes R, Chapman A, Rubinstein D, Stears J, Johnson A, Gabow P: Recurrent intracranial aneurysms (ICA) in autosomal dominant polycystic kidney disease (ADPKD). Stroke 27:178, 1996 (abstr).
40. Huston J III, Nichols DA, Luetmer PH, Goodwin JT, Meyer FB, Wiebers DO, Weaver AL: Blinded prospective evaluation of sensitivity of MR angiography to known intracranial aneurysms: Importance of aneurysm size. AJNR Am J Neuroradiol 15:16071614, 1994.
41. Huston J III, Torres VE, Sulivan PP, Offord KP, Wiebers DO: Value of magnetic resonance nngiography for the detection of intracranial aneurysms in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 3:1871-1877, 1993.
42. Huston J III, Torres VE, Wiebers DO, Schievink WI: Follow-up of unruptured intracranial aneurysms in autosomal dominant polycystic kidney disease by magnetic resonance angiography. J Am Soc Nephrol 7:2135-2141, 1996.
43. liada H, Segawa C, Takahashi T, Aoki S, Demachi H, Hondo H: Screening for occult intracranial aneurysms in autosomal dominant polycystic kidney disease (ADPKD) with MR angiography. J Am Soc Nephrol 6:722, 1995 (abstr).
44. Juvela S, Porras M, Heiskanen O: Natural history of unruptured intracranial aneurysms: A long-term follow-up study. J Neurosurg 79:174-182, 1993.
45. Kahn E, Markowitz J, Duffy L, Kenigsberg K, Davis JG, Daum F: Berry aneurysms, cirrhosis, pulmonary emphysema, and bilateral symmetrical cerebral calcifications: A new syndrome. Am J Med Genet 3[Suppl]:343-356, 1987.
46. Kimberling WJ, Fain PR, Kenyon JB, Goldgar D, Sujansky E, Gabow PA: Linkage heterogeneity of autosomal dominant polycystic kidney disease. N Engl J Med 319:913-918, 1988.
47. Kimberling WJ, Kumar S, Gabow PA, Kenyon JB, Connolly CJ, Somlo S: Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4ql3-q23. Genomics 18:467-472, 1993.
48. King JT Jr, Berlin JA, Flamm ES: Morbidity and mortality from elective surgery for asymptomatic, unruptured, intracranial aneurysms: A meta-analysis. J Neurosurg 81:837-842, 1994.
49. Klucznik RP, Carrier DA, Pyka R, Haid RW: Placement of a ferromagnetic intracerebral aneurysm clip in a magnetic field with a fatal outcome. Radiology 187:855-856, 1993.
50. Korogi Y, Takahashi M, Mabuchi N, Miki H, Fujiwara S, Horikawa Y: Intracranial aneurysms: Diagnostic accuracy of three-dimensional, Fourier transform, time-of-flight MR angiography. Radiology 193:181-186, 1994.
51. Kuivaniemi H, Prockop DJ, Wu Y, Madhatheri SL, Kleiner! C, Early JJ, Jokinen A, Stolle C, Majamaa K, Myllylä W, Norrgârd 0, Schievink WI, Mokri B, Fukawa O, ter Berg HWM, de Paepe A, Lozano AM, Leblanc R, Ryynänen M, Baxter BT, Shikata H, Ferrell RE, Tromp G: Exclusion of mutations in the gene for Type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: Results from sequence analysis of the coding sequences of Type III collagen from 55 unrelated patients. Neurology 43:2652-2658, 1993.
52. Kulla L, Deymeer F, Smith TW, Weiner M, Mullins TF III: Intracranial dissecting and saccular aneurysms in polycystic kidney disease. Arch Neurol 39:776-778, 1982.
53. Leblanc R, Melanson D, Tampieri D, Guttmann RD: Familial cerebral aneurysms: A study of 13 families. Neurosurgery 37: 633-639, 1995.
54. Lozano AM, Leblanc R: Familial intracranial aneurysms. J Neurosurg 66:522-528, 1987.
55. Majamaa K, Savolainen E-R, Myllylh W: Synthesis of structurally unstable Type III procollagen in patients with cerebral artery aneurysm. Biochim Biophys Acta 138:191-196, 1992.
56. Makos MM, McComb RD, Hart MN, Bennett DR: Alphaglucosidase deficiency and basilar artery aneurysm: Report of a sibship. Ann Neurol 22:629-633, 1987.
57. Martinez JR, Grantham JJ: Polycystic kidney disease: Etiology, pathogenesis, and treatment. Dis Mon 16:693-765, 1995.
58. Mayberg MR, Batjer HH, Dacey R, Diringer M, Haley EC, Heros RC, Sternau LL, Torner J, Adams HP, Feinberg W, Thies W: Guidelines for the management of aneurysmal subarachnoid hemorrhage: A statement for health care professionals from a special \vriting group of the Stroke Council, American Heart Association. Stroke 25:2315-2328, 1994.
59. McCormick WF, Acosta-Rua GJ: The size of intracranial saccular aneurysms: An autopsy study. J Neurosurg 33:422-427, 1970.
60. Milewicz DM, Grossfield J, Cao S-N, Kielty C, Covitz W, Jewett T: A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome. J Clin Invest 95:2372-2378, 1995.
61. Motuo Fotso MJ, Brunon J, Outhel R, Fischer G: Anévrysmes familiaux, anévrysmes multiples et anévrysmes 'de novo': A propos de deux observations. Neurochirurgie 39:225-230, 1993.
62. Neil-Dwyer G, Bartlett JR, Nicholls AC, Pope FM: Collagen deficiency and ruptured cerebral aneurysms: A clinical and biochemical study. J Neurosurg 59:16-20, 1983.
63. Norrgârd 0, Ängquist K-A, Fodstad H, Forsell A, Lindberg M: Intracranial aneurysms and heredity. Neurosurgery 20:236-239, 1987.
64. Norrgârd 0, Beckman G, Beckman L, Cedergren B, Fodstad H, Ängquist K-A: Genetic markers in patients \vilh intracranial aneurysms. Hum Hered 37:255-259, 1987.
65. North KN, Whiteman DAH, Pepin MG, Byers PH: Cerebrovascular complications in Ehlers-Danlos syndrome Type IV. Ann Neurol 38:960-964, 1995.
66. Obuchowski NA, Modic MT, Magdinec M: Current implications for the efficacy of noninvasive screening for occult intracranial aneurysms in patients with a family history of aneurysms. J Neurosurg 83:42-49, 1995.
67. Ogawa T, Okudera T, Noguchi K: Cerebral aneurysms: Evaluation with three-dimensional CT angiography. AJNR Am J Neuroradiol 17:447-454, 1996.
68. 0stergaard JR, Bruun-Petersen G, Lamm LU: HLA antigens and complement types in patients with intracranial saccular aneurysms. Tissue Antigens 28:176-181, 1986.
69. 0stergaard JR, Oxlund H: Collagen Type III deficiency in patients with rupture of intracranial saccular aneurysms. J Neurosurg 67:690-696, 1987.
70. Parekh HC, Gurusinghe NT, Sharma RR: Cerebral berry aneurysms in identical twins: A case report. Surg Neurol 38:277-279, 1992.
71. Peters DJ, Spruit L, Saris JJ, Ravine D, Sandkuijl LA, Fossdal R, Boersma J, van Eijk R, Norby S, Constantinou-Deltas CD, Piérides A, Brissenden JE, Franls RR, van Ommen G-JB, Breuning MH: Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease. Nature Genet 5:359362, 1993.
72. Phillips LH II, Whisnant JP, O'Fallon WM, Sundt TM Jr: The unchanging pattern of subarachnoid hemorrhage in a community. Neurology 30:1034-1040, 1980.
73. Poli P, Peillon C, Lahda E, Watelet J, Testart J: Anévrysmes intracraniens multiples en rapport avec une maladie de Recklinghausen: A propos d'un cas. J Mal Vase 19:253-255,1994.
74. Pope FM, Kendall BE, Slapak GI, Kapoor R, McDonald WI, Compston DAS, Mitchell R, Hope DT, Millar-Craig MW, Dean JCS, Johnston AW, Lynch PG, Sarathchandra P, Narcisi P, Nicholls AC, Richards AJ, Mackenzie JL: Type III collagen mutations cause fragile cerebral arteries. Br J Neurosurg 5:551-574,1991.
75. Puchner MJ, Lohmann F, Valdueza JM, Siepmann G, Freckmann N: Monozygotic twins not identical with respect to the existence of intracranial aneurysms: A case report. Surg Neurol 41:284289, 1994.
76. Pyeritz RE: The Marfan syndrome, in Royce PM, Steinmann B (eds): Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects. New York, Wiley-Liss, 1993, pp 437-468.
77. Pyeritz RE, Fishman EK, Bernhardt BA, Siegelman SJ: Durai ectasia is a common feature of the Marfan syndrome. Am J Hum Genet 43:726-732, 1988.
78. Rambaud J-C, Galian A, Touchard G, Morel-Maroger L, Mikol J, van Effenterre G: Digestive tract and renal small vessel hyalinosis, idiopathic nonarteriosclerotic intracerebral calcifications, retinal ischémie syndrome, and phenotypic abnormalities: A new familial syndrome. Gastroenterology 90:930-938, 1986.
79. Reeders ST, Breuning MH, Davies KE, Nicholls RD, Jarman AP, Higgs DR, Pearson PL, Weatherall DJ: A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature 317:542-544,1985.
80. Reubi F: Neurofibromatosis et lésions vasculaires. Schweiz Med Wochenschr 75:463-465, 1945.
81. Riccardi VM: Neurofibromntosis: Phenotype, Natural History and Pathogcnesis. Baltimore, Johns Hopkins University Press, 1992, ed 2.
82. Roach ES, Zimmerman CF: Ehlers-Danlos syndrome, in Bogousslavsky J, Caplan L (eds): Stroke Syndromes. Cambridge, Cambridge University Press, 1995, pp 491-196.
83. Ronkainen A, Hernesniemi J, Ryynänen M: Familial subarachnoid hemorrhage in East Finland, 1977-1990. Neurosurgery 33: 787-797,1993.
84. Ronkainen A, Hernesniemi J, Tromp G: Special features of familial intracranial aneurysms: Report of 215 familial aneurysms. Neurosurgery 37:43-47, 1995.
85. Ronkainen A, Puranen MI, Hernesniemi JA, Vanninen RL, Partanen PL, Saari JT, Vainio PA, Ryynänen M: Intracranial aneurysms: MR angiographie screening in 400 asymptomatic individuals with increased familial risk. Radiology 195:35-40, 1995.
86. Rose BS, Pretorius DL: Dissecting basilar artery aneurysm in Marfan syndrome: Case report. AJNR Am J Neuroradiol 12:503504, 1991.
87. Ruggieri PM, Poulos N, Masaryk TJ, Ross JS, Obuchowski NA, Awad IA, Braun WE, Nally J, Lewin JS, Modic MT: Occult intracranial aneurysms in polycystic kidney disease: Screening with MRA. Radiology 191:33-39, 1994.
88. Ryba M, Grieb P, Podobinska I, Iwanska K, Pastuszko M, Gorski A: HLA antigens and intracranial aneurysms. Acta Neurochir (Wien)116:l-5, 1992.
89. Sakai LY, Keene DR, Engvall E: Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol 103:2499-2509, 1986.
90. Sasaki J, Miura S, Ohishi H, Kikuchi K: Neurofibromatosis associated with multiple intracranial vascular lesions: Stenosis of the internal carotid artery and peripheral aneurysm of Huebner's artery-Report of a case [in Japanese]. No Shinkei Geka 23:813-817, 1995.
91. Schievink WI, Piepgras DG: Cervical vertebral artery aneurysms and arteriovenous fistulae in neurofibromatosis Type 1: Case reports. Neurosurgery 29:760-765, 1991.
92. Schievink WI, Schaid DJ: Prognosis of familial versus nonfamilial aneurysmal subarachnoid hemorrhage. Stroke 27:340-341, 1996.
93. Schievink WI, Björnsson J, Piepgras DG: Coexistence of fibromuscular dysplasia and cystic medial necrosis in a patient with Marfan's syndrome and bilateral carotid artery dissections. Stroke 25:2492-2496,1994.
94. Schievink WI, de Waal LP, Hageman LM, van der Werf DJM: Intracranial aneurysm and HLA-DR2. J Neurol Neurosurg Psychiatry 51:883, 1988 (letter).
95. Schievink WI, Huston J III, Torres VE, Marsh WR: Intracranial cysts in autosomal dominant polycystic kidney disease. J Neurosurg 83:1004-1007, 1995.
96. Schievink WI, Katzmann JA, Piepgras DG, Schaid DJ: Alpha-1antitrypsin phenotypes among patients with intracranial aneurysms. J Neurosurg 84:781-784, 1996.
97. Schievink WI, Limburg M, Dreissen JJR, Peelers FLM, ter Berg HWM: Screening for unruptured familial intracranial aneurysms: Subarachnoid hemorrhage 2 years after angiography negative for aneurysms. Neurosurgery 29:434-438,1991.
98. Schievink WI, Limburg M, Oorthuys JWE, Fleury P, Pope FM: Cerebrovascular disease in Ehlers-Danlos syndrome Type IV. Stroke 21:626-632,1990.
99. Schievink WI, Michels W, Piepgras DG: Neurovascular manifestations of heritable connective tissue disorders: A review. Stroke 25:889-903, 1994.
100. Schievink WI, Parisi JE, Piepgras DG, Michels W: Genetic aspects of cerebral aneurysms. Presented at the 21st International Joint Conference on Stroke and Cerebral Circulation, San Antonio, Texas, January 26, 1996.
101. Schievink WI, Piepgras DG, Earnest FIV, Gordon H: Spontaneous carotid-cavernous fistulae in Ehlers-Danlos syndrome Type IV: Case report. J Neurosurg 74:881-889,1991.
102. Schievink WI, Piepgras DG, Wirth FP: Rupture of previously documented small asymptomatic saccular intracranial aneurysms: Report of three cases. J Neurosurg 76:1019-1024, 1992.
103. Schievink WI, Schaid DJ, Michels W, Piepgras DG: Familial aneurysmal subarachnoid hemorrhage: A community-based study. J Neurosurg 83:426-429, 1995.
104. Schievink WI, Schaid DJ, Rogers HM, Piepgras DG, Michels W: On the inheritance of intracranial aneurysms. Stroke 25:20282037,1994.
105. Schievink WI, Torres VE, Piepgras DG, Wiebers DO: Saccular intracranial aneurysms in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 3:88-95,1992.
106. Schievink WI, Torres VE, Wiebers DO, Huston J III: Intracranial arterial dolichoectasia in autosomal dominant polycystic kidney disease. J Am Soc Nephrol (in press).
107. Schwartz RB, Tice HM, Hooten SM, Hsu L, Stieg PE: Evaluation of cerebral aneurysms with helical CT: Correlation with conventional angiography and MR angiography. Radiology 192:717722, 1994.
108. Shen MH, Harper PS, Upadhyaya M: Molecular genetics of neurofibromatosis Type l (NF1). J Med Genet 33:2-17, 1996.
109. Shinton R, Palsingh J, Williams B: Cerebral haemorrhage and berry aneurysm: Evidence from a family for a pattern of autosomal dominant inheritance. J Neurol Neurosurg Psychiatry 54:838-840, 1991.
110. Sobata E, Ohkuma H, Suzuki S: Cerebrovascular disorders associated with von Recklinghausen's neurofibrornatosis: A case report. Neurosurgery 22:544-549, 1988.
111. Steinmann B, Royce PM, Superti-Furga A: The Ehlers-Danlos syndromes, in Royce PM, Steinmann B (eds): Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects. New York, Wiley-Liss, 1993, pp 351-407.
112. Strang RR: Age, sex, and ABO blood group distributions of 150 patients with cerebral arteriovenous aneurysms. J Med Genet 4:29-30, 1967.
113. Suter W: Das kongenitale Aneurysma der basalen Hirnarterien und Cystennieren. Schweiz Med Wochenschr 79:471-476,1949.
114. ter Berg HWM, Bijlsma JB, Willemse J: Familial occurrence of intracranial aneurysms in childhood: A case report and review of the literature. Neuropedialrics 18:227-230,1987.
115. ter Berg HWM, Dippel DWJ, Limburg M, Schievink WI, van Gijn J: Familial intracranial aneurysms: A review. Stroke 23:10241030, 1992.
116. Uranishi R, Ochiai C, Okuno S, Nagai M: Cerebral aneurysms associated with von Recklinghausen neurofibrornatosis: Report of two cases [in Japanese]. No Shinkei Geka 23:237-242, 1995.
117. van Dijk MA, Chang PC, Peters DJM, Breuning MH: Intracranial aneurysms in polycystic kidney disease linked to chromosome 4. J Am Soc Nephrol 6:1670-1673,1995.
118. Wang PS, Longstreth WTJr, Koepsell TD: Subarachnoid hemorrhage and family history: A population-based case-control study. Arch Neurol 52:202-204, 1995.
119. Wiebers DO, Torres VE: Screening for unruptured intracranial aneurysms in autosomal dominant polycystic kidney disease. N Engl J Med 327:953-955,1992.
120. Wiebers DO, Whisnant JP, Sundt TM Jr, O'Fallon WM: The significance of unruptured intracranial aneurysms. J Neurosurg 66:23-29,1987.