Recurrent Encephalopathy as a Form of Presentation of Transport Protein Particle Complex 11-Related Disease: A Family Matter.

BACKGROUND

Transport protein particle complex 11 (TRAPPC11)-related disease, with autosomal recessive inheritance, exhibits a multisystemic involvement that goes widely beyond muscle weakness. Poor growth, psychomotor development delay, intellectual disability, microcephaly, ophthalmic involvement, and movement disorders are some of the typical features. Elevated serum creatine kinase levels are present in all previously reported TRAPPC11 c.1278+5G > A variant cases.

METHODS

Clinical characterization of three siblings from a Roma family with TRAPPC11-related disease, all harboring a homozygous c.1287+5G > A variant.

RESULTS

The older siblings presented typical features of the disease, including significant microcephaly, intellectual delay, and psychomotor regression precipitated by infections. Ataxia was consistently observed across all cases, albeit with varying severity. None of the cases had clinical signs compatible with muscular dystrophy. Notably, despite sharing the same mutation, the siblings exhibited remarkable phenotypic variability, with the youngest sibling displaying a milder phenotype.

CONCLUSIONS

This case series elucidates the intricate presentation of TRAPPopathies and underscores its phenotypic diversity, emphasizing the influence of the implicated deleterious variant. This study contributes to our understanding of TRAPPC11-related disease and highlights the importance of recognizing and characterizing phenotypic variability in this genetic disorder.