Miller-Dieker syndrome (MDS)

Neuronal migration disorder [DS:H01835]

Guerrini R, Marini C

Genetic malformations of cortical development.

Exp Brain Res 173:322-33 (2006)
DOI:10.1007/s00221-006-0501-z

Kerjan G, Gleeson JG

Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.

Trends Genet 23:623-30 (2007)
DOI:10.1016/j.tig.2007.09.003

Spalice A, Parisi P, Nicita F, Pizzardi G, Del Balzo F, Iannetti P

Neuronal migration disorders: clinical, neuroradiologic and genetics aspects.

Acta Paediatr 98:421-33 (2009)
DOI:10.1111/j.1651-2227.2008.01160.x

Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, Day-Salvatore DL, Horner M, Lu XY, Sahoo T, Yanagawa Y, Beaudet AL, Cheung SW, Martinez S, Lupski JR, Reiner O

Increased LIS1 expression affects human and mouse brain development.

Nat Genet 41:168-77 (2009)
DOI:10.1038/ng.302

Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Nat Genet 26:93-6 (2000)
DOI:10.1038/79246

Poirier K, Keays DA, Francis F, Saillour Y, Bahi N, Manouvrier S, Fallet-Bianco C, Pasquier L, Toutain A, Tuy FP, Bienvenu T, Joriot S, Odent S, Ville D, Desguerre I, Goldenberg A, Moutard ML, Fryns JP, van Esch H, Harvey RJ, Siebold C, Flint J, Beldjord C, Chelly J

Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).

Hum Mutat 28:1055-64 (2007)
DOI:10.1002/humu.20572

Bakircioglu M, Carvalho OP, Khurshid M, Cox JJ, Tuysuz B, Barak T, Yilmaz S, Caglayan O, Dincer A, Nicholas AK, Quarrell O, Springell K, Karbani G, Malik S, Gannon C, Sheridan E, Crosier M, Lisgo SN, Lindsay S, Bilguvar K, Gergely F, Gunel M, Woods CG

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.

Am J Hum Genet 88:523-35 (2011)
DOI:10.1016/j.ajhg.2011.03.019

Radmanesh F, Caglayan AO, Silhavy JL, Yilmaz C, Cantagrel V, Omar T, Rosti B, Kaymakcalan H, Gabriel S, Li M, Sestan N, Bilguvar K, Dobyns WB, Zaki MS, Gunel M, Gleeson JG

Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities.

Am J Hum Genet 92:468-74 (2013)
DOI:10.1016/j.ajhg.2013.02.005

Mishra-Gorur K, Caglayan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F, Akgumus GT, Nishimura S, Han W, Tu S, Baran B, Gumus H, Dilber C, Zaki MS, Hossni HA, Riviere JB, Kayserili H, Spencer EG, Rosti RO, Schroth J, Per H, Caglar C, Caglar C, Dolen D, Baranoski JF, Kumandas S, Minja FJ, Erson-Omay EZ, Mane SM, Lifton RP, Xu T, Keshishian H, Dobyns WB, Chi NC, Sestan N, Louvi A, Bilguvar K, Yasuno K, Gleeson JG, Gunel M

Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors.

Neuron 84:1226-39 (2014)
DOI:10.1016/j.neuron.2014.12.014

Magen D, Ofir A, Berger L, Goldsher D, Eran A, Katib N, Nijem Y, Vlodavsky E, Tzur S, Behar DM, Fellig Y, Mandel H

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Hum Genet 134:305-14 (2015)
DOI:10.1007/s00439-014-1522-5

Jerber J, Zaki MS, Al-Aama JY, Rosti RO, Ben-Omran T, Dikoglu E, Silhavy JL, Caglar C, Musaev D, Albrecht B, Campbell KP, Willer T, Almuriekhi M, Caglayan AO, Vajsar J, Bilguvar K, Ogur G, Abou Jamra R, Gunel M, Gleeson JG

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.

Am J Hum Genet 99:1181-1189 (2016)
DOI:10.1016/j.ajhg.2016.09.007

Dobyns WB, Aldinger KA, Ishak GE, Mirzaa GM, Timms AE, Grout ME, Dremmen MHG, Schot R, Vandervore L, van Slegtenhorst MA, Wilke M, Kasteleijn E, Lee AS, Barry BJ, Chao KR, Szczaluba K, Kobori J, Hanson-Kahn A, Bernstein JA, Carr L, D'Arco F, Miyana K, Okazaki T, Saito Y, Sasaki M, Das S, Wheeler MM, Bamshad MJ, Nickerson DA, Engle EC, Verheijen FW, Doherty D, Mancini GMS

MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance.

Am J Hum Genet 103:1009-1021 (2018)
DOI:10.1016/j.ajhg.2018.10.019

Tsai MH, Muir AM, Wang WJ, Kang YN, Yang KC, Chao NH, Wu MF, Chang YC, Porter BE, Jansen LA, Sebire G, Deconinck N, Fan WL, Su SC, Chung WH, Almanza Fuerte EP, Mehaffey MG, Ng CC, Chan CK, Lim KS, Leventer RJ, Lockhart PJ, Riney K, Damiano JA, Hildebrand MS, Mirzaa GM, Dobyns WB, Berkovic SF, Scheffer IE, Tsai JW, Mefford HC

Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly.

Neuron 106:237-245.e8 (2020)
DOI:10.1016/j.neuron.2020.01.027

Leger PL, Souville I, Boddaert N, Elie C, Pinard JM, Plouin P, Moutard ML, des Portes V, Van Esch H, Joriot S, Renard JL, Chelly J, Francis F, Beldjord C, Bahi-Buisson N

The location of DCX mutations predicts malformation severity in X-linked lissencephaly.

Neurogenetics 9:277-85 (2008)
DOI:10.1007/s10048-008-0141-5

Kitamura K, Yanazawa M, Sugiyama N, Miura H, Iizuka-Kogo A, Kusaka M, Omichi K, Suzuki R, Kato-Fukui Y, Kamiirisa K, Matsuo M, Kamijo S, Kasahara M, Yoshioka H, Ogata T, Fukuda T, Kondo I, Kato M, Dobyns WB, Yokoyama M, Morohashi K

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.

Nat Genet 32:359-69 (2002)
DOI:10.1038/ng1009

Russell LJ, Weaver DD, Bull MJ, Weinbaum M

In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence.

Am J Med Genet 17:509-21 (1984)
DOI:10.1002/ajmg.1320170213

Guven A, Gunduz A, Bozoglu TM, Yalcinkaya C, Tolun A

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.

Neurogenetics 13:189-94 (2012)
DOI:10.1007/s10048-012-0326-9

Behunova J, Zavadilikova E, Bozoglu TM, Gunduz A, Tolun A, Yalcinkaya C

Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequence.

Clin Dysmorphol 19:107-18 (2010)
DOI:10.1097/MCD.0b013e32833946e9