Associated Papers
Neuroradiological Phenotype Expansion of the Siddiqi Syndrome: A Case Report.
Trilla P et al.
Cellular and Molecular Neurobiology, 2026
FITM2-Related Siddiqi Syndrome in Two Iranian Siblings.
Ahmadi R et al.
Clinical Case Reports, 2025
Partial loss of FITM2 function causes hereditary spastic paraplegia.
Salazar-Villacorta A et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant.
Lin Y et al.
Clinical Genetics, 2022
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