Heritability and de novo mutations in oesophageal atresia and tracheoesophageal fistula aetiology

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Abstract

Tracheoesophageal Fistula (TOF) is a congenital anomaly for which the cause is unknown in the majority of patients. OA/TOF is a variable feature in many (often mono-) genetic syndromes. Research using animal models targeting genes involved in candidate pathways often result in tracheoesophageal phenotypes. However, there is limited overlap in the genes implicated by animal models and those found in OA/TOF-related syndromic anomalies. Knowledge on affected pathways in animal models is accumulating, but our understanding on these pathways in patients lags behind. If an affected pathway is associated with both animals and patients, the mechanisms linking the genetic mutation, affected cell types or cellular defect, and the phenotype are often not well under-stood. The locus heterogeneity and the uncertainty of the exact heritability of OA/TOF results in a relative low diagnostic yield. OA/TOF is a sporadic finding with a low familial recurrence rate. As parents are usually unaffected, de novo dominant mutations seems to be a plausible explanation. The survival rates of patients born with OA/TOF have increased substantially and these patients start families; thus, the detection and a proper interpretation of these dominant inherited pathogenic variants are of great importance for these patients and for our understanding of OA/TOF aetiology.

Original languageEnglish
Article number1595
Number of pages18
JournalGenes
Volume12
Issue number10
DOIs
Publication statusPublished - 10 Oct 2021

Bibliographical note

Funding Information:
This work was supported by the Sophia Foundation for Scientific Research (grant numbers 493 (to D.T. and A.d.K.) and S13-09 (to D.T., A.d.K. and E.B.)).

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

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