Marfan syndrome associated with moyamoya phenomenon and aortic dissection

Acta Neurochirurgica

Volumn 141, Issue 6, 1999, Pages 663-665

  Terada, Tomoaki ^a   Yokote, H ^a   Tsuura, M ^a   Nakai, K ^a   Ohshima, A ^b   Itakura, T ^a  

^a Department of Neurological Surgery ^*  (Japan)

^b WAKAYAMA MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; HUMAN; MALE; MARFAN SYNDROME; MOYAMOYA DISEASE; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ANEURYSM, DISSECTING; AORTIC ANEURYSM; FATAL OUTCOME; HUMANS; MALE; MARFAN SYNDROME; MOYAMOYA DISEASE;

EID: 0033010888     PISSN: 00016268     EISSN: None     Source Type: Journal    
DOI: 10.1007/s007010050358     Document Type: Article

References (5)

1. 1. Dietz HC, Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A (1991b) Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 352: 337-339
2. 2. Paepe AD, Devereux RB, Dietz HC, Hennekam RCM, Pyeritz RE (1996) Revised diagnostic criteria for the Marfan syndrome. Am J Med Genet 62: 417-426
3. 3. Richman DP, Watts HG, Parson D, Schmid K, Glimcher MJ (1977) Familial moyamoya associated with biochemical abnormalities of connective tissue. Neurology (abstract). 27: 382
4. 4. Rose BS, Pretorius DL (1991) Dissecting basilar artery aneurysm in Marfan syndrome: case report, AJNR 12: 503-504
5. 5. Rovira M, Torrent O, Ruscalleda J (1975) Etiology of moyamoya disease, acquired or congenital. Acta Radio 347: 229-240