Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

lissencephaly with cerebellar hypoplasia type A - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

lissencephaly with cerebellar hypoplasia type A

MONDO:0015034

Overview

Lissencephaly with cerebellar hypoplasia type A (LCHa) is a form of lissencephaly with cerebellar hypoplasia that encompasses classical lissencephaly with thickened cortical gray matter with either no discernible gradient, a gradient with posterior predominance, or a gradient with anterior predominance, and cerebellar vermis hypoplasia.

ResearchLimited published research (4 articles)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for lissencephaly with cerebellar hypoplasia type A.

4 publications have been identified in PubMed for lissencephaly with cerebellar hypoplasia type A. Research spans Case Report / Case Series (75%) and Basic Science / Preclinical (25%).

Recent Publications

Newman JM (2025). [PMID: 40974083](https://pubmed.ncbi.nlm.nih.gov/40974083/). *J Neuropathol Exp Neurol*. [Case Report / Case Series]
Moirangthem A (2025). [PMID: 40186457](https://pubmed.ncbi.nlm.nih.gov/40186457/). *Clin Genet*. [Basic Science / Preclinical]
Sharma PK (2024). [PMID: 39228958](https://pubmed.ncbi.nlm.nih.gov/39228958/). *Radiol Case Rep*. [Case Report / Case Series]
Hayashi K (2024). [PMID: 39452687](https://pubmed.ncbi.nlm.nih.gov/39452687/). *Neurol Int*. [Case Report / Case Series]

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 7:55 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:100011

GARD

Genetic and Rare Diseases Info Center

GARD:19731

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

lissencephaly with cerebellar hypoplasia type A

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team