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

Nose and Nasal Cavity01:24

Nose and Nasal Cavity

The nose is composed of an observable exterior segment (external nose) and an internal segment within the skull known as the nasal cavity (internal nose). The external nose, visible on the face, consists of a framework of bone and hyaline cartilage enveloped in skin and muscle and lined with a mucous membrane. This structure is supported by the frontal bone, nasal bones, and maxillary bone and is supplemented by a cartilaginous framework comprising the septal nasal cartilage, lateral nasal...
Cranial Bones: Lateral View01:27

Cranial Bones: Lateral View

The lateral view of the cranium is dominated by temporal, sphenoid, and ethmoid bones.
The temporal bone forms the lower lateral side of the skull. The temporal bone is subdivided into several regions. The flattened upper portion is the squamous portion of the temporal bone. Below this area and projecting anteriorly is the zygomatic process of the temporal bone, which forms the posterior portion of the zygomatic arch. Posteriorly is the mastoid portion of the temporal bone. Projecting...
Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the anterior...
Prosopagnosia01:24

Prosopagnosia

Prosopagnosia, also known as face blindness, is the inability to recognize faces. In severe cases, individuals with prosopagnosia may not recognize close family members, including parents and spouses, by their faces. For instance, someone with prosopagnosia might walk past their child in a crowd, only realizing their mistake upon noticing their child's distinctive backpack or favorite jacket. Prosopagnosia specifically impairs facial recognition, while the recognition of other objects or...
Olfactory Receptors: Location and Structure01:03

Olfactory Receptors: Location and Structure

The process of olfaction, also known as the sense of smell, is a sophisticated chemical response system. The specialized sensory neurons that facilitate this process, known as olfactory receptor neurons, are situated in an upper segment of the nasal cavity, known as the olfactory epithelium. Olfactory sensory neurons are bipolar, with their dendrites extending from the epithelium's apex into the mucus that lines the nasal cavity. Airborne molecules, when inhaled, traverse the olfactory...
Cryptococcal Meningitis01:27

Cryptococcal Meningitis

Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...

You might also read

Related Articles

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

Sort by
Same author

Surgical Management of Choanal Atresia: Two Classic Cases and Review of the Literature.

Cureus·2022
Same author

Apnea-hypopnea index severity as an independent predictor of post-tonsillectomy respiratory complications in pediatric patients: A retrospective study.

Ear, nose, & throat journal·2021
Same author

The role of CDHR3 in susceptibility to otitis media.

Journal of molecular medicine (Berlin, Germany)·2021
Same author

Thyroglossal duct cyst anterior to the sternum: a novel presentation of a common lesion.

BMJ case reports·2020
Same author

Bilateral Cervical Pilomatricoma: A Diagnostic Dilemma for the Pediatric Otolaryngologist.

Ear, nose, & throat journal·2020
Same author

Multi-omic studies on missense PLG variants in families with otitis media.

Scientific reports·2020

Related Experiment Video

Updated: Jul 16, 2026

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model
08:03

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model

Published on: November 4, 2025

Congenital nasal malformations.

Wasyl Szeremeta1, Tejas Dinesh Parikh, Jeffrey S Widelitz

  • 1Temple University School of Medicine, Philadelphia, PA, USA. wasyl@ent.temple.edu

Otolaryngologic Clinics of North America
|March 10, 2007
PubMed
Summary

Congenital nose malformations impact children's well-being. Understanding nasal development is key to diagnosing and managing these conditions and associated syndromes.

Area of Science:

  • Pediatric Plastic Surgery
  • Craniofacial Anomalies
  • Embryology

Background:

  • Congenital nasal abnormalities present a spectrum of functional and anatomic challenges.
  • These anomalies can range from subtle to overt, impacting a child's physiological and psychological health.
  • Severe cases may manifest as life-threatening emergencies in newborns.

Purpose of the Study:

  • To provide a comprehensive overview of congenital nasal malformations.
  • To correlate nasal embryology and development with common clinical presentations.
  • To discuss syndromes frequently associated with nasal abnormalities.

Main Methods:

  • Review of nasal embryology and developmental processes.
  • Clinical case discussions of significant congenital nasal abnormalities.

More Related Videos

Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

Related Experiment Videos

Last Updated: Jul 16, 2026

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model
08:03

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model

Published on: November 4, 2025

Transuterine Fetal Tracheal Occlusion Model in Mice
06:31

Transuterine Fetal Tracheal Occlusion Model in Mice

Published on: February 5, 2021

  • Syndromic association analysis for common nasal anomalies.
  • Main Results:

    • Nasal development is crucial for understanding congenital defects.
    • Various congenital nasal malformations require specific diagnostic and management strategies.
    • Identification of common syndromes involving nasal abnormalities aids in comprehensive patient care.

    Conclusions:

    • A thorough understanding of nasal embryology is fundamental for diagnosing congenital nasal malformations.
    • Management requires a tailored approach based on the specific anomaly and potential syndromic involvement.
    • Early recognition and intervention are vital for improving outcomes in affected children.