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Case Reports
. 2010 Jul;19(3):164-165.
doi: 10.1097/MCD.0b013e3283387b3b.

KBG syndrome associated with periventricular nodular heterotopia

Renske Oegema  1 , Rachel Schot, Marie Claire Y de Wit, Maarten H Lequin, Rianne Oostenbrink, Irenaeus F M de Coo, Grazia M S Mancini
Affiliations
Case Reports

KBG syndrome associated with periventricular nodular heterotopia

Renske Oegema et al. Clin Dysmorphol. 2010 Jul.
No abstract available

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References

    1. Andrade D 2009. Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain. Hum Genet 126:173–193.
    1. Brancati F, Sarkozy A, Dallapiccola B 2006. KBG syndrome. Orphanet J Rare Dis 1:50.
    1. Kumar H, Prabhu N, Cameron A 2009. KBG syndrome: review of the literature and findings of 5 affected patients. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 108:e72–e79.
    1. Skjei KL, Martin MM, Slavotinek AM 2007. KBG syndrome: report of twins, neurological characteristics, and delineation of diagnostic criteria. Am J Med Gen Part A 143A:292–300.

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