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Pyriform aperture enlargement in all aspects.
E Esen1, N Bayar Muluk2, N Altintoprak3
1ENT Clinics,Kocaeli Derince Training and Research Hospital,Kocaeli,Turkey.
The Journal of Laryngology and Otology
|February 28, 2017
Summary
Congenital nasal pyriform aperture stenosis, a condition affecting facial bone structure, can be linked to craniofacial issues. Treatment options range from non-surgical to operative, with outcomes depending on associated conditions.
Area of Science:
- Craniofacial anatomy and development
- Pediatric Otorhinolaryngology
- Medical Genetics
Background:
- The pyriform aperture is central to facial bone structure, formed by the nasal bone and maxillae.
- Congenital nasal pyriform aperture stenosis may be associated with various craniofacial abnormalities.
- This review comprehensively covers pyriform aperture stenosis and enlargement.
Purpose of the Study:
- To review all aspects of pyriform aperture stenosis and enlargement.
- To detail the anatomical and developmental context of the pyriform aperture.
- To discuss diagnostic and therapeutic considerations for congenital nasal pyriform aperture stenosis.
Main Methods:
- A comprehensive literature search was performed.
- Key areas reviewed include pyriform aperture definition, nasal development, and stenosis/enlargement.
- The review synthesizes existing knowledge on the condition.
Main Results:
- Holoprosencephaly is a common associated abnormality, indicating midline developmental deficiency.
- The exact cause of nasal pyriform aperture stenosis is not fully understood.
- Treatment is individualized, balancing non-surgical and operative approaches based on severity and airway security.
Conclusions:
- Operative outcomes for pyriform aperture stenosis are generally favorable.
- Prognosis is significantly influenced by coexisting neural and endocrine conditions.
- This paper provides an in-depth evaluation of the nasal pyriform aperture.

