Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Aneurysm I: Introduction01:30

Aneurysm I: Introduction

14
An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
14

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Abstracts Association Tunisienne de Médecine Néonatale (ATMN).

La Tunisie medicale·2026
Same author

Treacher Collins syndrome: A case report and review of literature.

Clinical case reports·2023
Same author

Arabic adaptation of the Edinburgh cognitive and behavioural Amyotrophic lateral sclerosis screen (ECAS-AR).

Revue neurologique·2022
Same author

Clinical predictors of disease progression in a cohort of Tunisian progressive Multiple Sclerosis.

Multiple sclerosis and related disorders·2021
Same author

Utility of salivary gland ultrasonography in primary Sjögren syndrome.

The Netherlands journal of medicine·2020
Same author

Multiple sclerosis 2017 McDonald criteria are also relevant for Tunisians.

Multiple sclerosis and related disorders·2020

Related Experiment Video

Updated: Jul 22, 2025

State of the Art Cranial Ultrasound Imaging in Neonates
10:02

State of the Art Cranial Ultrasound Imaging in Neonates

Published on: February 2, 2015

24.4K

Congenital Arhinia: A Neonatal Case Report.

Nadia Kolsi1,2, K Mekki1,2, Ch Regaieg1,2

  • 1Faculty of Medicine, University of Sfax, Sfax, Tunisia.

Ear, Nose, & Throat Journal
|July 22, 2023
PubMed
Summary

Congenital arhinia, a rare nasal absence, presents significant neonatal respiratory distress. This case report highlights the challenges in managing this malformation and reviews existing literature.

Keywords:
arhiniacongenital malformationmultidisciplinary medical careprognosis

More Related Videos

Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

3.2K
A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
07:50

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

Published on: September 20, 2018

15.9K

Related Experiment Videos

Last Updated: Jul 22, 2025

State of the Art Cranial Ultrasound Imaging in Neonates
10:02

State of the Art Cranial Ultrasound Imaging in Neonates

Published on: February 2, 2015

24.4K
Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

3.2K
A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
07:50

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

Published on: September 20, 2018

15.9K

Area of Science:

  • Medical Genetics
  • Pediatric Surgery
  • Neonatology

Background:

  • Congenital arhinia, or complete absence of the nose, is an extremely rare congenital malformation.
  • Fewer than 100 cases have been documented globally, making it a significant clinical rarity.
  • The condition poses immediate life-threatening risks, primarily severe respiratory distress in newborns.

Purpose of the Study:

  • To report a case of congenital arhinia in a female neonate.
  • To discuss the clinical presentation and initial management of this rare condition.
  • To review the existing literature on congenital arhinia and its management strategies.

Main Methods:

  • Case report of a female newborn diagnosed with congenital arhinia.
  • Review of relevant medical literature on congenital arhinia.
  • Analysis of immediate neonatal airway management strategies.

Main Results:

  • Successful stabilization of the neonatal airway was achieved.
  • The case highlights the critical need for prompt respiratory support in affected infants.
  • Literature review underscores the lack of standardized management protocols.

Conclusions:

  • Congenital arhinia necessitates urgent airway management for survival.
  • The rarity of this condition complicates the development of defined treatment guidelines.
  • Further research and case sharing are crucial for improving patient outcomes.