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Results 1 - 8 of 8 for Lissencephaly 2
  1. Lissencephaly with cerebellar hypoplasia 
    ... the disorder in their family. LCH LIS2 LIS3 Lissencephaly 2 Lissencephaly 3 Lissencephaly syndrome, Norman-Roberts type Norman- ... Cobblestone lissencephaly National Organization for Rare Disorders (NORD) LISSENCEPHALY 2; LIS2 LISSENCEPHALY 3; LIS3 PubMed Chang BS, Duzcan ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  2. X-linked lissencephaly with abnormal genitalia 
    ... linked traits to their sons. LISX2 X-linked lissencephaly 2 X-linked lissencephaly with ambiguous genitalia XLAG XLISG ... abnormal genitalia National Organization for Rare Disorders (NORD) LISSENCEPHALY, X-LINKED, 2; LISX2 PubMed Bonneau D, Toutain A, Laquerriere A, ...
    https://medlineplus.gov/...ked-lissencephaly-with-abnormal-genitalia - Genetics
  3. Isolated lissencephaly sequence 
    ... in the neuropathology and pathophysiology of type I lissencephaly. Acta Neuropathol. 2011 Feb;121(2):149-70. doi: 10.1007/s00401-010-0768- ... disorders. Curr Neurol Neurosci Rep. 2011 Apr;11(2):171-8. doi: ... spectrum of mutations and relationships with malformation severity. ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  4. Subcortical band heterotopia 
    ... AE, Cushion TD, Pilz DT. The genetics of lissencephaly. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):198-210. doi: 10.1002/ajmg.c.31402. ...
    https://medlineplus.gov/.../condition/subcortical-band-heterotopia - Genetics
  5. Miller-Dieker syndrome 
    ... Clark GD, Prokscha A, Dobyns WB, Eichele G. Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development. Mech Dev. 2000 Apr;92(2):263-71. doi: 10.1016/s0925-4773(00) ...
    https://medlineplus.gov/genetics/condition/miller-dieker-syndrome - Genetics
  6. Fukuyama congenital muscular dystrophy 
    ... this condition have a brain abnormality called cobblestone lissencephaly, in which ... Fukuyama ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  7. Walker-Warburg syndrome 
    ... that this problem with neuronal migration causes cobblestone lissencephaly in children with Walker-Warburg syndrome. Less is ... BRAIN AND EYE ANOMALIES), TYPE A, 2; MDDGA2 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  8. Baraitser-Winter syndrome 
    ... folds and grooves. Less commonly, affected individuals have lissencephaly, which is similar to ... National Organization for ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics