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limb body wall complex - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

limb body wall complex

MONDO:0016528

Also known as:LBWC syndromeCyllosomasaplasia of the cord

Overview

Limb body wall complex (LBWC) is characterized by severe multiple congenital anomalies in the fetus with exencephaly/encephalocele, thoraco- and/or abdominoschisis (anterior body wall defects) and limb defects, with or without facial clefts.

Diagnosis

Biomarker and diagnostic research for limb body wall complex has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

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 limb body wall complex.

110 publications have been identified in PubMed for limb body wall complex. Kisho has analyzed 40 by research type. Research spans Review / Meta-Analysis (55%), Epidemiology / Natural History (18%), and Case Report / Case Series (10%).

Research Type	Count	% of Total
Research summaries	22	55%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 10:41 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:2369

GARD

Genetic and Rare Diseases Info Center

GARD:3251

Questions for Your Care Team

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limb body wall complex

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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