Anlaufstelle für Eltern und Angehörige an Lissenzephalie leidender Kinder e.V. (LISS) Assigned diseases:
In the following you will find the diseases that this support group organisation focuses on:
Classic lissencephaly
Cobblestone lissencephaly
Cobblestone lissencephaly without muscular or ocular involvement
Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
Isolated lissencephaly type 1 without known genetic defects
Lissencephaly
Lissencephaly due to LIS1 mutation
Lissencephaly due to TUBA1A mutation
Lissencephaly type 1 due to doublecortin gene mutation
Lissencephaly type 3
Lissencephaly type 3-familial fetal akinesia sequence syndrome
Lissencephaly type 3-metacarpal bone dysplasia syndrome
Lissencephaly with cerebellar hypoplasia
Lissencephaly with cerebellar hypoplasia type A
Lissencephaly with cerebellar hypoplasia type B
Lissencephaly with cerebellar hypoplasia type C
Lissencephaly with cerebellar hypoplasia type D
Lissencephaly with cerebellar hypoplasia type E
Lissencephaly with cerebellar hypoplasia type F
Microlissencephaly
Miller-Dieker syndrome
Neu-Laxova syndrome
Other syndrome with lissencephaly as a major feature
Periventricular nodular heterotopia