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Biomarker and diagnostic research for multiple congenital anomalies/dysmorphic syndrome has been reported in the published literature.
No clinical trials have been registered for multiple congenital anomalies/dysmorphic syndrome.
251 publications have been identified in PubMed for multiple congenital anomalies/dysmorphic syndrome. Research spans Case Report / Case Series (39%), Review / Meta-Analysis (21%), and Basic Science / Preclinical (20%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 99 | 39% |
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:46 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Research summaries
53 |
21% |
Laboratory research | 50 | 20% |
Disease patterns and progression | 36 | 14% |
Testing and diagnosis research | 7 | 3% |
Clinical study results | 4 | 2% |
Other research | 2 | 1% |
Hindermann M (2026). [PMID: 41729076](https://pubmed.ncbi.nlm.nih.gov/41729076/). *JCI Insight*. [Basic Science / Preclinical]
Ozcelik F (2026). [PMID: 42104006](https://pubmed.ncbi.nlm.nih.gov/42104006/). *Neurogenetics*. [Review / Meta-Analysis]
AlMoallem B (2026). [PMID: 42074478](https://pubmed.ncbi.nlm.nih.gov/42074478/). *Genes (Basel)*. [Case Report / Case Series]
Taha O (2026). [PMID: 41208733](https://pubmed.ncbi.nlm.nih.gov/41208733/). *J Pediatr Orthop*. [Epidemiology / Natural History]
Gąsiorowska J (2026). [PMID: 42023627](https://pubmed.ncbi.nlm.nih.gov/42023627/). *Pediatr Endocrinol Diabetes Metab*. [Review / Meta-Analysis]
Vanneste M (2026). [PMID: 41266135](https://pubmed.ncbi.nlm.nih.gov/41266135/). *J Med Genet*. [Diagnostic / Biomarker]
Langer S (2026). [PMID: 41513036](https://pubmed.ncbi.nlm.nih.gov/41513036/). *J Pediatr Surg*. [Review / Meta-Analysis]
Elsherbini A (2026). [PMID: 41689580](https://pubmed.ncbi.nlm.nih.gov/41689580/). *J Hand Surg Am*. [Review / Meta-Analysis]
Young RE (2026). [PMID: 40931319](https://pubmed.ncbi.nlm.nih.gov/40931319/). *Clinical genetics*. [Basic Science / Preclinical]
Sabbagh Q (2026). [PMID: 41882293](https://pubmed.ncbi.nlm.nih.gov/41882293/). *Eur J Hum Genet*. [Basic Science / Preclinical]