Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly

Congenital hyporhinia, also known as partial arhinia, is a very rare congenital abnormality of nasal embryogenesis with unknown etiology. It is commonly associated with other craniofacial anomalies which are thought to be caused by an absent or rudimentary nose. A 3‐h‐old neonate presented to our fa...

Descripción completa

Detalles Bibliográficos
Autores principales: Mlay, Kenneth, Chussi, Desderius, Mtenga, Philbert, Shija, Peter, Msele, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017404/
https://www.ncbi.nlm.nih.gov/pubmed/36937628
http://dx.doi.org/10.1002/ccr3.7099
_version_ 1784907575442014208
author Mlay, Kenneth
Chussi, Desderius
Mtenga, Philbert
Shija, Peter
Msele, Angela
author_facet Mlay, Kenneth
Chussi, Desderius
Mtenga, Philbert
Shija, Peter
Msele, Angela
author_sort Mlay, Kenneth
collection PubMed
description Congenital hyporhinia, also known as partial arhinia, is a very rare congenital abnormality of nasal embryogenesis with unknown etiology. It is commonly associated with other craniofacial anomalies which are thought to be caused by an absent or rudimentary nose. A 3‐h‐old neonate presented to our facility with hypoplastic nasal pyramid, hypertelorism, microcephaly, and micrognathia, a case of congenital hyporhinia with associated anomalies is presented and the embryology and literature review are discussed.
format Online
Article
Text
id pubmed-10017404
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-100174042023-03-17 Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly Mlay, Kenneth Chussi, Desderius Mtenga, Philbert Shija, Peter Msele, Angela Clin Case Rep Case Report Congenital hyporhinia, also known as partial arhinia, is a very rare congenital abnormality of nasal embryogenesis with unknown etiology. It is commonly associated with other craniofacial anomalies which are thought to be caused by an absent or rudimentary nose. A 3‐h‐old neonate presented to our facility with hypoplastic nasal pyramid, hypertelorism, microcephaly, and micrognathia, a case of congenital hyporhinia with associated anomalies is presented and the embryology and literature review are discussed. John Wiley and Sons Inc. 2023-03-15 /pmc/articles/PMC10017404/ /pubmed/36937628 http://dx.doi.org/10.1002/ccr3.7099 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mlay, Kenneth
Chussi, Desderius
Mtenga, Philbert
Shija, Peter
Msele, Angela
Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title_full Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title_fullStr Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title_full_unstemmed Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title_short Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly
title_sort congenital hyporhinia with associated malformations: case report of a rare congenital anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017404/
https://www.ncbi.nlm.nih.gov/pubmed/36937628
http://dx.doi.org/10.1002/ccr3.7099
work_keys_str_mv AT mlaykenneth congenitalhyporhiniawithassociatedmalformationscasereportofararecongenitalanomaly
AT chussidesderius congenitalhyporhiniawithassociatedmalformationscasereportofararecongenitalanomaly
AT mtengaphilbert congenitalhyporhiniawithassociatedmalformationscasereportofararecongenitalanomaly
AT shijapeter congenitalhyporhiniawithassociatedmalformationscasereportofararecongenitalanomaly
AT mseleangela congenitalhyporhiniawithassociatedmalformationscasereportofararecongenitalanomaly

Ejemplares similares