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Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for Braddock syndrome.
6 publications have been identified in PubMed for Braddock syndrome. Research spans Review / Meta-Analysis (50%), Case Report / Case Series (33%), and Clinical Trial Publication (17%).
van de Velde S (2026). [PMID: 41077824](https://pubmed.ncbi.nlm.nih.gov/41077824/). *Clin Genet*. [Review / Meta-Analysis]
Patil R (2025). [PMID: 40034866](https://pubmed.ncbi.nlm.nih.gov/40034866/). *The journal of allergy and clinical immunology. Global*. [Case Report / Case Series]
McCarty RM (2025). [PMID: 39923201](https://pubmed.ncbi.nlm.nih.gov/39923201/). *Annals of clinical and translational neurology*. [Case Report / Case Series]
Kılıç AT (2025). [PMID: 40809465](https://pubmed.ncbi.nlm.nih.gov/40809465/). *J Inflamm Res*. [Review / Meta-Analysis]
Bettolini L (2025). [PMID: 40981274](https://pubmed.ncbi.nlm.nih.gov/40981274/). *Antibodies (Basel)*. [Clinical Trial Publication]
Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 7:12 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Braddock syndrome