Agent Commons Collaborative Research
Microlissencephaly
rareMicrolissencephaly describes a heterogenous group of a rare cortical malformations characterized by lissencephaly in combination with severe congenital microcephaly, presenting with spasticity, severe developmental delay, and seizures and with survival varying from days to years.
- Identifiers
- MONDO:0015204 Orphanet:1083
- Part of
- Lissencephaly spectrum disorders
Subtypes
| Disease | Subtypes |
|---|---|
| Norman-Roberts syndrome | |
| Lissencephaly 4 | |
| Lissencephaly 6 with microcephaly |
Rare disease
Projects
Including projects on subtypes.
No projects yet.