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A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype

The transforming growth factor-β-activated kinase 1 (TAK1) encoded by mitogen-activated protein kinase kinase kinase 7 (MAP3K7) is widely expressed and participates in multiple molecular and cellular processes, including growth, differentiation, inflammation, and apoptosis. Pathogenic variants in MA...

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Autores principales: AbuBakr, Fatima, Jeffries, Lauren, Ji, Weizhen, McGrath, James M., Lakhani, Saquib A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304360/
https://www.ncbi.nlm.nih.gov/pubmed/32299812
http://dx.doi.org/10.1101/mcs.a005207
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author AbuBakr, Fatima
Jeffries, Lauren
Ji, Weizhen
McGrath, James M.
Lakhani, Saquib A.
author_facet AbuBakr, Fatima
Jeffries, Lauren
Ji, Weizhen
McGrath, James M.
Lakhani, Saquib A.
author_sort AbuBakr, Fatima
collection PubMed
description The transforming growth factor-β-activated kinase 1 (TAK1) encoded by mitogen-activated protein kinase kinase kinase 7 (MAP3K7) is widely expressed and participates in multiple molecular and cellular processes, including growth, differentiation, inflammation, and apoptosis. Pathogenic variants in MAP3K7 have recently been associated with two disorders: cardiospondylocarpofacial syndrome (CSCFS) and frontometaphyseal dysplasia 2 (FMD2). To date, all small in-frame deletions and splice variants in MAP3K7 have been associated with CSCFS, whereas missense variants have been reported in both CSCFS and FMD2. Here, we present a patient with a novel heterozygous likely pathogenic variant, c.125_127del, p.(Val42del), in MAP3K7, only the sixth variant associated with CSCFS to be described in the literature. Although this patient has a phenotype that is most consistent with that of CSCFS, including valvular heart disease, short stature, fusions of the spine and bones of the hands and feet, and certain facial dysmorphisms, he interestingly has some features reported previously in FMD2 but not CSCFS. These include flexion contractures of the elbow and widely spaced first and second toes, highlighting new points of overlap between these two syndromes. We additionally point out features in the patient presented here that are rare but recurrent among CSCFS patients previously reported in the literature, as well as a new distinctive cutaneous finding not previously reported.
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spelling pubmed-73043602020-06-23 A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype AbuBakr, Fatima Jeffries, Lauren Ji, Weizhen McGrath, James M. Lakhani, Saquib A. Cold Spring Harb Mol Case Stud Rapid Communication The transforming growth factor-β-activated kinase 1 (TAK1) encoded by mitogen-activated protein kinase kinase kinase 7 (MAP3K7) is widely expressed and participates in multiple molecular and cellular processes, including growth, differentiation, inflammation, and apoptosis. Pathogenic variants in MAP3K7 have recently been associated with two disorders: cardiospondylocarpofacial syndrome (CSCFS) and frontometaphyseal dysplasia 2 (FMD2). To date, all small in-frame deletions and splice variants in MAP3K7 have been associated with CSCFS, whereas missense variants have been reported in both CSCFS and FMD2. Here, we present a patient with a novel heterozygous likely pathogenic variant, c.125_127del, p.(Val42del), in MAP3K7, only the sixth variant associated with CSCFS to be described in the literature. Although this patient has a phenotype that is most consistent with that of CSCFS, including valvular heart disease, short stature, fusions of the spine and bones of the hands and feet, and certain facial dysmorphisms, he interestingly has some features reported previously in FMD2 but not CSCFS. These include flexion contractures of the elbow and widely spaced first and second toes, highlighting new points of overlap between these two syndromes. We additionally point out features in the patient presented here that are rare but recurrent among CSCFS patients previously reported in the literature, as well as a new distinctive cutaneous finding not previously reported. Cold Spring Harbor Laboratory Press 2020-06 /pmc/articles/PMC7304360/ /pubmed/32299812 http://dx.doi.org/10.1101/mcs.a005207 Text en © 2020 AbuBakr et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits reuse and redistribution, except for commercial purposes, provided that the original author and source are credited.
spellingShingle Rapid Communication
AbuBakr, Fatima
Jeffries, Lauren
Ji, Weizhen
McGrath, James M.
Lakhani, Saquib A.
A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title_full A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title_fullStr A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title_full_unstemmed A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title_short A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
title_sort novel variant in map3k7 associated with an expanded cardiospondylocarpofacial syndrome phenotype
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304360/
https://www.ncbi.nlm.nih.gov/pubmed/32299812
http://dx.doi.org/10.1101/mcs.a005207
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