Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype

T Apuhan1, A Saglam Kubra1, M Yilmaz1

  • 1Department of Medical Genetics, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.

Summary

Monoallelic KIF11 variants cause Microcephaly with or without Chorioretinopathy, Lymph-edema, or Impaired Intellectual Development (MCLMR) syndrome. This study reveals extreme clinical heterogeneity and novel findings, including prenatal lymphedema and craniosynostosis, expanding the KIF11 disease spectrum.

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