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Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing

Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing
Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing
Individuals from three families ascertained in Bogota, Colombia, showing syndromic phenotypes, including cleft lip and/or palate, were exome sequenced. In each case sequencing revealed underlying causal variation confirming or establishing diagnoses. The findings include very rare and novel variants providing insights into genotype and phenotype relationships. These include the molecular diagnosis of an individual with Nager syndrome and a family exhibiting an atypical Incontinentia Pigmenti phenotype with a missense mutation in IKBKG. IKBKG mutations are typically associated with pre-term male death but this variant is associated with survival for 8–15 days. The third family exhibits unusual phenotypic features and the proband received a provisional diagnosis of Pierre Robin Sequence (PRS). Affected individuals share a novel deleterious mutation in IRF6. Mutations in IRF6 cause Van der Woude and Popliteal pterygium syndrome and contribute to nonsyndromic cleft lip phenotypes but have not previously been associated with a PRS phenotype. Exome sequencing followed by in silico screening to identify candidate causal variant(s), and functional assay in some cases, offers a powerful route to establishing molecular diagnoses. This approach is invaluable for conditions showing phenotypic and/or genetic heterogeneity including cleft lip and/or palate phenotypes where many underlying causal genes have not been identified.
cleft lip and palate, exome sequencing, incontinentia pigmenti, nager syndrome, pierre robin sequence, syndromic disease
0009-9163
441-449
Pengelly, Reuben
af97c0c1-b568-415c-9f59-1823b65be76d
Upstill-Goddard, Rosanna
db6c4d69-2a08-4185-9fc8-cad65f27dde6
Arias, Liliana
f44e52e3-21f5-4beb-a12b-42bb0b73afd1
Martinez, Julio
f24a598b-6222-4475-95e3-4ec9445f5d1f
Gibson, Jane
855033a6-38f3-4853-8f60-d7d4561226ae
Knut, Marcin
68d387d0-9b44-48d1-91c6-310f7470cdc2
Collins, Amanda L.
877712f2-b733-45e0-891e-784245bb7ce6
Ennis, Sarah
7b57f188-9d91-4beb-b217-09856146f1e9
Collins, Andrew
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Briceno, Ignacio
aaf8caee-1ab9-4291-b3ec-0eadd182b75e
Pengelly, Reuben
af97c0c1-b568-415c-9f59-1823b65be76d
Upstill-Goddard, Rosanna
db6c4d69-2a08-4185-9fc8-cad65f27dde6
Arias, Liliana
f44e52e3-21f5-4beb-a12b-42bb0b73afd1
Martinez, Julio
f24a598b-6222-4475-95e3-4ec9445f5d1f
Gibson, Jane
855033a6-38f3-4853-8f60-d7d4561226ae
Knut, Marcin
68d387d0-9b44-48d1-91c6-310f7470cdc2
Collins, Amanda L.
877712f2-b733-45e0-891e-784245bb7ce6
Ennis, Sarah
7b57f188-9d91-4beb-b217-09856146f1e9
Collins, Andrew
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Briceno, Ignacio
aaf8caee-1ab9-4291-b3ec-0eadd182b75e

Pengelly, Reuben, Upstill-Goddard, Rosanna, Arias, Liliana, Martinez, Julio, Gibson, Jane, Knut, Marcin, Collins, Amanda L., Ennis, Sarah, Collins, Andrew and Briceno, Ignacio (2015) Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole-exome sequencing. Clinical Genetics, 88 (5), 441-449. (doi:10.1111/cge.12547). (PMID:25441681)

Record type: Article

Abstract

Individuals from three families ascertained in Bogota, Colombia, showing syndromic phenotypes, including cleft lip and/or palate, were exome sequenced. In each case sequencing revealed underlying causal variation confirming or establishing diagnoses. The findings include very rare and novel variants providing insights into genotype and phenotype relationships. These include the molecular diagnosis of an individual with Nager syndrome and a family exhibiting an atypical Incontinentia Pigmenti phenotype with a missense mutation in IKBKG. IKBKG mutations are typically associated with pre-term male death but this variant is associated with survival for 8–15 days. The third family exhibits unusual phenotypic features and the proband received a provisional diagnosis of Pierre Robin Sequence (PRS). Affected individuals share a novel deleterious mutation in IRF6. Mutations in IRF6 cause Van der Woude and Popliteal pterygium syndrome and contribute to nonsyndromic cleft lip phenotypes but have not previously been associated with a PRS phenotype. Exome sequencing followed by in silico screening to identify candidate causal variant(s), and functional assay in some cases, offers a powerful route to establishing molecular diagnoses. This approach is invaluable for conditions showing phenotypic and/or genetic heterogeneity including cleft lip and/or palate phenotypes where many underlying causal genes have not been identified.

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More information

e-pub ahead of print date: 1 December 2014
Published date: November 2015
Keywords: cleft lip and palate, exome sequencing, incontinentia pigmenti, nager syndrome, pierre robin sequence, syndromic disease
Organisations: Human Development & Health, Centre for Biological Sciences

Identifiers

Local EPrints ID: 372604
URI: http://eprints.soton.ac.uk/id/eprint/372604
ISSN: 0009-9163
PURE UUID: d7c79105-1970-47f7-a80e-e5e0a4e24931
ORCID for Reuben Pengelly: ORCID iD orcid.org/0000-0001-7022-645X
ORCID for Jane Gibson: ORCID iD orcid.org/0000-0002-0973-8285
ORCID for Sarah Ennis: ORCID iD orcid.org/0000-0003-2648-0869
ORCID for Andrew Collins: ORCID iD orcid.org/0000-0001-7108-0771

Catalogue record

Date deposited: 16 Dec 2014 16:36
Last modified: 15 Mar 2024 03:48

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Contributors

Author: Reuben Pengelly ORCID iD
Author: Rosanna Upstill-Goddard
Author: Liliana Arias
Author: Julio Martinez
Author: Jane Gibson ORCID iD
Author: Marcin Knut
Author: Amanda L. Collins
Author: Sarah Ennis ORCID iD
Author: Andrew Collins ORCID iD
Author: Ignacio Briceno

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