Expansion of the Phenotype of You‐Hoover‐Fong Syndrome and Possible Increased Risk of Cancer

You-Hoover-Fong syndrome (YHFS) is a rare autosomal recessive disorder characterized by global developmental delay, microcephaly, dysmorphic facial features, and a spectrum of neurodevelopmental abnormalities. YHFS is caused by pathogenic variants in TELO2, a gene involved in regulation of the cell cycle. To date, 29 individuals with YHFS have been reported and none of them has been reported to develop tumors. We describe two siblings with YHFS both presenting with bilateral acoustic nerve agenesis, microcephaly, and dysmorphic features. Notably, one sibling developed hepatoblastoma at the age of 7.5 years. Clinical exome sequencing revealed in both siblings compound heterozygous variants in the TELO2 gene. Although the development of hepatoblastoma might be coincidental, given the role of TELO2 in cell cycle, we suspect YHFS might be associated with an increased cancer susceptibility. Further cases are needed to confirm whether YHFS is associated with an increased risk of cancer.

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Publication Details

Journal
American Journal of Medical Genetics Part A
Published
2024-12-20
DOI
https://doi.org/10.1002/ajmg.a.63966
Citations
1
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.29
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article

Expansion of the Phenotype of You‐Hoover‐Fong Syndrome and Possible Increased Risk of Cancer

Chiara Paolella, Vincenzo Nigro, Massimo Eraldo Abate, Iris Scala et al.
1 citations
American Journal of Medical Genetics Part A
Cancer Genomics and Diagnostics
0.29
article

Expansion of the Phenotype of You‐Hoover‐Fong Syndrome and Possible Increased Risk of Cancer

Chiara Paolella, Vincenzo Nigro, Massimo Eraldo Abate, Iris Scala, Nicola Brunetti‐Pierri, Alessandro De Falco, Fabiola De Gregorio
article en
1 citations

Abstract

You-Hoover-Fong syndrome (YHFS) is a rare autosomal recessive disorder characterized by global developmental delay, microcephaly, dysmorphic facial features, and a spectrum of neurodevelopmental abnormalities. YHFS is caused by pathogenic variants in TELO2, a gene involved in regulation of the cell cycle. To date, 29 individuals with YHFS have been reported and none of them has been reported to develop tumors. We describe two siblings with YHFS both presenting with bilateral acoustic nerve agenesis, microcephaly, and dysmorphic features. Notably, one sibling developed hepatoblastoma at the age of 7.5 years. Clinical exome sequencing revealed in both siblings compound heterozygous variants in the TELO2 gene. Although the development of hepatoblastoma might be coincidental, given the role of TELO2 in cell cycle, we suspect YHFS might be associated with an increased cancer susceptibility. Further cases are needed to confirm whether YHFS is associated with an increased risk of cancer.

American Journal of Medical Genetics Part AVol. 197(5)
University of Campania "Luigi Vanvitelli" (IT), Federico II University Hospital (IT), Santobono Children's Hospital (IT), Scuola Superiore Meridionale (IT), Telethon Institute Of Genetics And Medicine (IT), University of Naples Federico II (IT)
Good health and well-being
Openalex Percentile: Top 37%
Cancer Genomics and Diagnostics
0.29
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Expansion of the Phenotype of You‐Hoover‐Fong Syndrome and Possible Increased Risk of Cancer — Chiara Paolella, Vincenzo Nigro, et al. · American Journal of Medical Genetics Part A (2024) | TGRS Research Map | TGRS