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Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma

Congenital hypoplasia of depressor angularis oris muscle (CHDAOM) is an uncommon cause of asymmetric crying facies in neonates. Although its etiology is mostly unknown, it has been increasingly recognized as a marker for the presence of other less easily identifiable congenital abnormalities associa...

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Autores principales: Parfianowicz, Dominic, Uchendu, Uchendu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138455/
https://www.ncbi.nlm.nih.gov/pubmed/32269891
http://dx.doi.org/10.7759/cureus.7213
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author Parfianowicz, Dominic
Uchendu, Uchendu
author_facet Parfianowicz, Dominic
Uchendu, Uchendu
author_sort Parfianowicz, Dominic
collection PubMed
description Congenital hypoplasia of depressor angularis oris muscle (CHDAOM) is an uncommon cause of asymmetric crying facies in neonates. Although its etiology is mostly unknown, it has been increasingly recognized as a marker for the presence of other less easily identifiable congenital abnormalities associated with genetic syndromes such as DiGeorge and Cayler syndrome. We report a unique case of a male neonate that highlights the necessity of judicious and accurate clinical documentation with the presence of CHDAOM to avoid unnecessary forms of subsequent work-up.
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spelling pubmed-71384552020-04-08 Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma Parfianowicz, Dominic Uchendu, Uchendu Cureus Family/General Practice Congenital hypoplasia of depressor angularis oris muscle (CHDAOM) is an uncommon cause of asymmetric crying facies in neonates. Although its etiology is mostly unknown, it has been increasingly recognized as a marker for the presence of other less easily identifiable congenital abnormalities associated with genetic syndromes such as DiGeorge and Cayler syndrome. We report a unique case of a male neonate that highlights the necessity of judicious and accurate clinical documentation with the presence of CHDAOM to avoid unnecessary forms of subsequent work-up. Cureus 2020-03-08 /pmc/articles/PMC7138455/ /pubmed/32269891 http://dx.doi.org/10.7759/cureus.7213 Text en Copyright © 2020, Parfianowicz et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Family/General Practice
Parfianowicz, Dominic
Uchendu, Uchendu
Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title_full Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title_fullStr Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title_full_unstemmed Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title_short Hypoplasia of Depressor Angularis Oris in a Male Neonate Associated with Cephalohematoma
title_sort hypoplasia of depressor angularis oris in a male neonate associated with cephalohematoma
topic Family/General Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138455/
https://www.ncbi.nlm.nih.gov/pubmed/32269891
http://dx.doi.org/10.7759/cureus.7213
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