Related Experiment Video
Updated: Aug 6, 2025

Method of Studying Palatal Fusion using Static Organ Culture
Published on: September 19, 2015
Congenital Palatal Fistula with Cleft of the Soft Palate
Johnson Uchechukwu Achebe1, Obinna Remigius Okwesili1, Okechukwu Oliver Onumaegbu1
1Department of Surgery, University of Nigeria Teaching Hospital, Ituku-Ozalla, Enugu State, Nigeria.
Insights
Congenital palatal fistula is a rare condition, often linked to submucous cleft palate. Early diagnosis and surgical repair, like Bardach
Area of Science:
- Pediatric surgery
- Craniofacial anomalies
- Congenital malformations
Background:
- Congenital palatal fistula is a rare oral malformation, distinct from acquired perforations often seen post-cleft palate repair.
- It is frequently associated with an underlying submucous cleft palate, a condition where the palate muscles and bone do not fully fuse.
- Diagnosis shortly after birth is uncommon, making such cases noteworthy.
Observation:
- A case report of a 3-year-old girl diagnosed with congenital palatal fistula shortly after birth.
- The patient also presented with a cleft of the soft palate.
- This highlights the coexistence of these congenital conditions.
Findings:
- Successful surgical repair of the palatal fistula and cleft palate was performed using Bardach's palatoplasty.
- The surgical intervention aimed to correct the anatomical defect.
Implications:
- Early diagnosis and surgical management are crucial for congenital palatal fistula.
- Post-operative speech therapy referral is important for optimizing functional outcomes.
- This case contributes to understanding the presentation and management of rare congenital palatal anomalies.
Abstract:
Congenital palatal fistula or perforation is rare, unlike the acquired form which commonly results from cleft palate repair. Congenital palatal fistulae are often associated with submucous cleft palate. Only a few of this fistulae are diagnosed shortly after birth. We present the case of a 3-year old girl with congenital palatal fistula coexisting with cleft of the soft palate that was noticed shortly after birth. The palate was repaired using Bardach's palatoplasty and the client was subsequently referred to a speech therapist.
Related Concept Videos
Oral Cavity
Teeth: The teeth are the hardest structures in our bodies. Humans have two sets of teeth throughout their lifetime: deciduous (baby) teeth and permanent teeth. Each tooth consists of several parts: the crown (visible part), the root (embedded in the jaw), enamel (hard outer...
Esophageal Perforation-I: Introduction
The location of esophageal perforation can vary, occurring anywhere along the esophagus....
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Esophageal Perforation-II: Clinical Manifestations and Management
Clinical Manifestations:
Cardiopulmonary Resuscitation II: ACLS Airway Management
Suctioning the Oropharyngeal Airway
After assembling the equipment, the nurse should practice hand hygiene and don appropriate PPE according to infection control guidelines to avoid the...

