polymicrogyria, bilateral perisylvian, autosomal recessive
MONDO:0014333Mondo
Findings
No curated finding names polymicrogyria, bilateral perisylvian, autosomal recessive yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
6 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Language impairmentHPOHP:0002463
- 5 of 5 reported patients
- Perisylvian polymicrogyriaHPOHP:0012650
- 5 of 5 reported patients
- SeizureHPOHP:0001250
- 5 of 5 reported patients
- Intellectual disabilityHPOHP:0001249
- 4 of 5 reported patients
- ExotropiaHPOHP:0000577
- 1 of 5 reported patients
- Motor delayHPOHP:0001270
- 0 of 5 reported patients
Where it sits
Other names
1 name
Resolves to: polymicrogyria, bilateral perisylvian, autosomal recessive
- Also called
- polymicrogyria, bilateral perisylvian