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craniosynostosis syndrome, autosomal recessive - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

craniosynostosis syndrome, autosomal recessive

MONDO:0011679

Also known as:autosomal recessive craniosynostosiscraniosynostosis, autosomal recessive

Overview

Autosomal recessive form of craniosynostosis.

Diagnosis

Biomarker and diagnostic research for craniosynostosis syndrome, autosomal recessive has been reported in the published literature.

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 craniosynostosis syndrome, autosomal recessive.

19 publications have been identified in PubMed for craniosynostosis syndrome, autosomal recessive. Research spans Case Report / Case Series (50%), Basic Science / Preclinical (28%), and Diagnostic / Biomarker (11%).

Research Type	Count	% of Total
Patient case studies	9	50%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:43 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:606529

Questions for Your Care Team

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craniosynostosis syndrome, autosomal recessive

Overview

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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