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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.
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.
Area of Science:
- Genetics and Genomics
- Human Molecular Genetics
- Developmental Biology
Background:
- Monoallelic variants in the KIF11 gene are linked to Microcephaly with or without Chorioretinopathy, Lymph-edema, or Impaired Intellectual Development (MCLMR) syndrome (OMIM:152950).
- The clinical spectrum and genetic underpinnings of KIF11-related disorders are not fully elucidated, necessitating further investigation into genotype-phenotype correlations.
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