Association of trisomy 9p and band heterotopia

Neurology

Volumn 53, Issue 2, 1999, Pages 430-432

  Federico, Antonio ^a,e   Tomasetti, P ^e   Zollino, M ^b   Diomedi, M ^c   Dotti, M T ^a   De Stefano, N ^a   Gualdi, G F ^c   Neri, G ^b   Gigli, G L ^d  

^a UNIVERSITY OF SIENA   (Italy)

^b CATHOLIC UNIVERSITY   (Italy)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d UNIVERSITY HOSPITAL OF UDINE   (Italy)

^e Associazione Anni Verdi   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CELL MIGRATION; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC IMAGING; FACE DYSMORPHIA; HETEROTOPIA; HUMAN; MALE; NERVE CELL; NUCLEAR MAGNETIC RESONANCE IMAGING; PARTIAL TRISOMY 9; PRIORITY JOURNAL;

EID: 0033595215     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.53.2.430     Document Type: Article

References (10)

1. Rethore MO, Larget-Piet L, Abonyi D, et al. Four cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity. Ann Genet 1970;13:217-232.
2. Scalise A, Placidi F, Diomedi M, Gigli GL. Trisomy 9p and epilepsy. Neurology 1998;50:313. Letter; comment.
3. Stern JM. The epilepsy of trisomy 9p (see comments). Neurology 1996;47:821-824.
4. Barkovich AJ, Jackson DE Jr., Boyer RS. Band heterotopias: a newly recognized neuronal migration anomaly. Radiology 1989;171:455-458.
5. Barkovich AJ, Guerrini R, Battaglia G, et al. Band heterotopia: correlation of outcome with magnetic resonance imaging parameters. Ann Neurol 1994;36:609-617.
6. Tarani L, Colloridi F, Raguso G, et al. Trisomy 9 mosaicism syndrome. A case report and review of the literature. Ann Genet 1994;37:14-20.
7. Golden JA, Schoene WC. Central nervous system malformations in trisomy 9. J Neuropathol Exp Neurol 1993;52:71-77.
8. Dobyns WB, Andermann E, Andermann F, et al. X-linked malformations of neuronal migration. Neurology 1996;47:331-339.
9. Gleeson JG, Allen KM, Fox JW, et al. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 1998;92:63-72.
10. Raymond AA, Fish DR, Sisodiya SM, Alsanjari N, Stevens JM, Shorvon SD. Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patients. Brain 1995;118:629-660.