Title |
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizures
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Published in |
Pediatric Research, June 2018
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DOI | 10.1038/s41390-018-0083-z |
Pubmed ID | |
Authors |
Jennifer A. Wambach, Daniel J. Wegner, Ping Yang, Marwan Shinawi, Dustin Baldridge, Ewelina Betleja, Joshua S. Shimony, David Spencer, Brian P. Hackett, Marisa V. Andrews, Thomas Ferkol, Susan K. Dutcher, Moe R. Mahjoub, F. Sessions Cole |
Abstract |
Biallelic deleterious variants in RTTN, which encodes rotatin, are associated with primary microcephaly, polymicrogyria, seizures, intellectual disability, and primordial dwarfism in human infants. We performed exome sequencing of an infant with primary microcephaly, pontocerebellar hypoplasia, and intractable seizures and his healthy, unrelated parents. We cultured the infant's fibroblasts to determine primary ciliary phenotype. We identified biallelic variants in RTTN in the affected infant: a novel missense variant and a rare, intronic variant that results in aberrant transcript splicing. Cultured fibroblasts from the infant demonstrated reduced length and number of primary cilia. Biallelic variants in RTTN cause primary microcephaly in infants. Functional characterization of primary cilia length and number can be used to determine pathogenicity of RTTN variants. |
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