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Scalp defects-postaxial polydactyly syndrome is characterized by congenital scalp defects and postaxial polydactyly type A.
Features include: Postaxial polydactyly type A and Aplasia cutis congenita of scalp.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for scalp defects-postaxial polydactyly syndrome.
5 publications have been identified in PubMed for scalp defects-postaxial polydactyly syndrome. Research spans Case Report / Case Series (80%) and Review / Meta-Analysis (20%).
Abdul Rahman N (2025). [PMID: 39863915](https://pubmed.ncbi.nlm.nih.gov/39863915/). *J Med Case Rep*. [Case Report / Case Series]
Lo Giudice M (2025). [PMID: 40565597](https://pubmed.ncbi.nlm.nih.gov/40565597/). *Genes (Basel)*. [Case Report / Case Series]
Jumei'an A (2024). [PMID: 38957254](https://pubmed.ncbi.nlm.nih.gov/38957254/). *Cureus*. [Case Report / Case Series]
Martins WD (2024). [PMID: 38770437](https://pubmed.ncbi.nlm.nih.gov/38770437/). *Autops Case Rep*. [Case Report / Case Series]
Lazea C (2024). [PMID: 38791606](https://pubmed.ncbi.nlm.nih.gov/38791606/). *Int J Mol Sci*. [Review / Meta-Analysis]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 6:55 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center