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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction.
1 publication has been identified in PubMed for autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction. Research spans Review / Meta-Analysis (100%).
Aynaashe A (2026). [PMID: 41621017](https://pubmed.ncbi.nlm.nih.gov/41621017/). *Amino Acids*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:56 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center