Isolated Lissencephaly Sequence

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Xu, C. Isolated Lissencephaly Sequence. Encyclopedia. Available online: https://encyclopedia.pub/entry/4197 (accessed on 27 September 2026).

Xu C. Isolated Lissencephaly Sequence. Encyclopedia. Available at: https://encyclopedia.pub/entry/4197. Accessed September 27, 2026.

Xu, Camila. "Isolated Lissencephaly Sequence" Encyclopedia, https://encyclopedia.pub/entry/4197 (accessed September 27, 2026).

Xu, C. (2020, December 23). Isolated Lissencephaly Sequence. In Encyclopedia. https://encyclopedia.pub/entry/4197

Xu, Camila. "Isolated Lissencephaly Sequence." Encyclopedia. Web. 23 December, 2020.

Isolated Lissencephaly Sequence

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/isolated-lissencephaly-sequence

Isolated lissencephaly sequence (ILS) is a condition that affects brain development before birth.

genetic conditions

References

de Wit MC, de Rijk-van Andel J, Halley DJ, Poddighe PJ, Arts WF, de Coo IF,Mancini GM. Long-term follow-up of type 1 lissencephaly: survival is related toneuroimaging abnormalities. Dev Med Child Neurol. 2011 May;53(5):417-21. doi:10.1111/j.1469-8749.2011.03937.x.
Dobyns WB. The clinical patterns and molecular genetics of lissencephaly andsubcortical band heterotopia. Epilepsia. 2010 Feb;51 Suppl 1:5-9. doi:10.1111/j.1528-1167.2009.02433.x.
Friocourt G, Marcorelles P, Saugier-Veber P, Quille ML, Marret S, Laquerrière A. Role of cytoskeletal abnormalities in the neuropathology and pathophysiologyof type I lissencephaly. Acta Neuropathol. 2011 Feb;121(2):149-70. doi:10.1007/s00401-010-0768-9.
Guerrini R, Parrini E. Neuronal migration disorders. Neurobiol Dis. 2010May;38(2):154-66. doi: 10.1016/j.nbd.2009.02.008.
Liu JS. Molecular genetics of neuronal migration disorders. Curr NeurolNeurosci Rep. 2011 Apr;11(2):171-8. doi: 10.1007/s11910-010-0176-5. Review.
Saillour Y, Carion N, Quelin C, Leger PL, Boddaert N, Elie C, Toutain A,Mercier S, Barthez MA, Milh M, Joriot S, des Portes V, Philip N, Broglin D,Roubertie A, Pitelet G, Moutard ML, Pinard JM, Cances C, Kaminska A, Chelly J,Beldjord C, Bahi-Buisson N. LIS1-related isolated lissencephaly: spectrum ofmutations and relationships with malformation severity. Arch Neurol. 2009Aug;66(8):1007-15. doi: 10.1001/archneurol.2009.149.
Spalice A, Parisi P, Nicita F, Pizzardi G, Del Balzo F, Iannetti P. Neuronalmigration disorders: clinical, neuroradiologic and genetics aspects. ActaPaediatr. 2009 Mar;98(3):421-33. doi: 10.1111/j.1651-2227.2008.01160.x.
Tian G, Jaglin XH, Keays DA, Francis F, Chelly J, Cowan NJ. Disease-associatedmutations in TUBA1A result in a spectrum of defects in the tubulin folding andheterodimer assembly pathway. Hum Mol Genet. 2010 Sep 15;19(18):3599-613. doi:10.1093/hmg/ddq276.
Verrotti A, Spalice A, Ursitti F, Papetti L, Mariani R, Castronovo A,Mastrangelo M, Iannetti P. New trends in neuronal migration disorders. Eur JPaediatr Neurol. 2010 Jan;14(1):1-12. doi: 10.1016/j.ejpn.2009.01.005.

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Subjects: Genetics & Heredity

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Entry Collection: MedlinePlus

Update Date: 23 Dec 2020

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