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Lichstenstein syndrome is characterized by frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for Lichtenstein syndrome.
5 publications have been identified in PubMed for Lichtenstein syndrome. Research spans Case Report / Case Series (50%), Clinical Trial Publication (25%), and Epidemiology / Natural History (25%).
Bittner R (2025). [PMID: 40097851](https://pubmed.ncbi.nlm.nih.gov/40097851/). *Surg Endosc*. [Epidemiology / Natural History]
Pielaciński K (2025). [PMID: 40929531](https://pubmed.ncbi.nlm.nih.gov/40929531/). *Pol Merkur Lekarski*. [Clinical Trial Publication]
Neff T (2025). [PMID: 40135014](https://pubmed.ncbi.nlm.nih.gov/40135014/). *Cureus*. [Case Report / Case Series]
Sadecka AI (2024). [PMID: 38947654](https://pubmed.ncbi.nlm.nih.gov/38947654/). *Cureus*. [Case Report / Case Series]
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 10:41 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Lichtenstein syndrome