Neuronal migration disorder

Synonyms
Brain dysgenesis
Brain dysplasia
Subtypes
Lissencephaly
Pachygyria
Polymicrogyria
May Be Caused by
3-hydroxyisobutyric aciduria
3-ketothiolase deficiency
3-methylglutaconic aciduria
Acalvaria with neurological abnormality
Acardia
Achondroplasia
Aicardi syndrome
Aminopterin fetopathy
Amnion rupture sequence with exencephaly
Anencephaly
Apert syndrome
Aplasia cutis congenita
Aprosencephaly
Atelencephaly
Beta-hydroxyisobutyric aciduria
Bobble-head doll syndrome
Brachmann-de Lange syndrome
Brain dysgenesis-focal calcification
Brainstem dysgenesis-cranial nerve involvement
CEDNIK syndrome
Cephaloskeletal dysplasia
Cerebro-oculo-facio-skeletal syndrome
Cerebro-oculo-muscular syndrome
Cerebrorenodigital syndrome
Chromosome abnormality
Chudley-McCullough syndrome
Craniotelencephalic dysplasia
CRASH syndrome
Dandy-Walker syndrome
De Morsier syndrome
DiGeorge syndrome
Double cortex syndrome
Dyssegmental dysplasia
Ectodermal dysplasia-cystic brain changes
Ehlers-Danlos syndrome
Encephalocraniocutaneous lipomatosis
Epidermal nevus syndrome
Eronen syndrome
Facial hemangioma-corticovascular dysplasia
Familial aplasia of the cerebellar vermis
Familial cerebellar hypoplasia and congenital lymphedema
Familial diffuse cortical dysplasia
Familial porencephaly
Familial schizencephaly
Fetal alcohol syndrome
FG syndrome
Foix-Chavany-Marie syndrome
Fontaine-Farriaux syndrome
Frontonasal dysplasia
Fryns syndrome
Fukuyama-type muscular
Galloway-Mowat syndrome
Glutaric acidemia type 1
Glutaric acidemia type 2
Gorlin syndrome
Hemimegalencephaly
Hereditary nodular heterotopia and mega cisterna magna
Holoprosencephaly
Hydrolethalus syndrome
Hypomelanosis of Ito
IBIDS syndrome
Incontinentia pigmenti
Iniencephaly
Joubert syndrome
Kallmann syndrome
Kearns-Sayre syndrome
Knobloch syndrome
Larson-like syndrome
Lhermitte-Duclos disease
Lissencephaly syndrome
Macrocephaly-cutis marmorata telangiectasia syndrome
Meckel syndrome
Methylmalonic acidemia
Miller-Dieker syndrome
Mulibrey nanism
Nephronophthisis-encephalopathy
Neu-Laxova syndrome
Nonketotic hyperglycinemia
Oculo-auriculo-vertebral spectrum
Orofaciodigital syndrome type 1
Orofaciodigital syndrome type 2
Pallister-Hall syndrome
Pascual-Castroviejo syndrome
Perisylvian syndrome
Peroxisomal disorder
Pfeiffer syndrome
Polycystic brain and ectodermal dysplasia
Premature chromatid separation
Pseudotrisomy 13 syndrome
Pyruvate dehydrogenase deficiency
Rhombencephalosynapsis
Saethre-Chotzen syndrome
Smith-Lemli-Opitz syndrome
Stoll-Charrow-Poznanski syndrome
Sulfite oxidase deficiency
Thanatophoric dysplasia
Trisomy 21
Van den Ende-Gupta syndrome
Walker-Warburg syndrome
West syndrome
X-linked pachygyria and agenesis of the corpus callosum
Zellweger syndrome

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