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Up to: Hereditary neurological disease · Disorder of development or morphogenesis · Congenital nervous system disorder

Lissencephaly spectrum disorders

The term lissencephaly covers a group of rare malformations sharing the common feature of anomalies in the appearance of brain convolutions (characterized by simplification or absence of folding) associated with abnormal organization of the cortical layers as a result of neuronal migration defects during embryogenesis.

0 trials tagged with this condition →

Baraitser-Winter cerebrofrontofacial syndrome 0 trials Sub-types →
Warburg micro syndrome 0 trials Sub-types →
X-linked lissencephaly with abnormal genitalia 0 trials
Classic lissencephaly 0 trials Sub-types →
Cobblestone lissencephaly 0 trials Sub-types →
Craniotelencephalic dysplasia 0 trials
Lissencephaly 10 0 trials
Lissencephaly 7 with cerebellar hypoplasia 0 trials
Lissencephaly 8 0 trials
Lissencephaly spectrum disorder with complex brainstem malformation 0 trials Sub-types →
Lissencephaly type 3 0 trials Sub-types →
Lissencephaly with cerebellar hypoplasia 0 trials Sub-types →
Massa casaer ceulemans syndrome 0 trials
Microlissencephaly 0 trials Sub-types →