Palatal and Alveolar Tissue Deficiency in Infants With Complete Unilateral Cleft Lip and Palate

Katy A Bednar1, David S Briss1, Mohamed S Bamashmous1,2

  • 1Orthodontics and Dentofacial Orthopedics, Henry M. Goldman School of Dental Medicine, Boston University, Boston, MA, USA.

Insights

Patients with unilateral cleft lip and palate (UCLP) have a significant intrinsic deficiency in palatal and alveolar tissue. This tissue deficiency is crucial for planning individualized treatments for UCLP patients.

Area of Science:

  • Craniofacial surgery
  • Pediatric dentistry
  • Plastic surgery
  • 3D imaging in medicine

Background:

  • Unilateral cleft lip and palate (UCLP) is a common congenital condition affecting facial development.
  • Accurate assessment of tissue deficiency is vital for effective surgical and orthodontic interventions.
  • Previous studies have focused on external facial features, with less emphasis on intrinsic palatal and alveolar tissue volumes.

Purpose of the Study:

  • To quantify and compare the intrinsic palatal and alveolar tissue surface area in infants with UCLP versus age-matched controls.
  • To determine if a correlation exists between cleft gap width and the extent of tissue deficiency.
  • To establish a baseline for understanding tissue deficits in UCLP for improved treatment planning.

Main Methods:

  • 3D surface area measurements were performed on digitized plaster casts of the maxilla from 22 UCLP infants and 37 non-cleft controls.
  • Specific anatomical landmarks were used to define and measure palatal and alveolar surface areas, including cleft segments.
  • Statistical analysis was employed to compare surface areas between groups and assess correlations.

Main Results:

  • Infants with UCLP exhibited a statistically significant reduction in palatal and alveolar surface area compared to non-cleft controls (P < .001).
  • A positive correlation was observed between the surface area of cleft segments and the width of the cleft gap.
  • The total palatal surface area, including the cleft gap, was significantly smaller in the UCLP group (P < .0001).

Conclusions:

  • A significant intrinsic deficiency in palatal and alveolar tissue is a characteristic of UCLP.
  • The degree of tissue deficiency should be a key consideration in developing patient-specific treatment strategies for UCLP.
  • This quantitative data supports the need for tailored surgical approaches to address tissue deficits in UCLP patients.
Abstract

Related Concept Videos

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
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,...
481
Unrenewable Cells00:50

Unrenewable Cells

In humans, the photoreceptor cells of the eye and sensory hair cells of the ear lack stem cells. These cells are thus unrenewable and cannot be replaced when they are damaged or destroyed.
Photoreceptors
The retina is composed of several layers and contains specialized cells called photoreceptors. The photoreceptors (rods and cones) change their membrane potential when stimulated by light energy. There are two types of photoreceptors—rods and cones—which differ in the shape of...
2.6K
Oral Cavity01:11

Oral Cavity

The oral cavity, or the mouth, is a complex structure in humans that plays a vital role in our day-to-day lives. Its role is not only in chewing and swallowing food; it also plays a role in speech and facial expressions.
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...
2.0K
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
421
Assessment of the Mouth01:26

Assessment of the Mouth

A thorough mouth assessment, including inspection and palpation of the lips, gums, tongue, tonsils, uvula, and pharynx, is crucial in detecting potential health issues. Diseases ranging from oral cancer to systemic conditions like diabetes could be identified early through careful oral examination. This article provides a detailed guide on conducting a comprehensive mouth assessment.
Mouth Inspection
The inspection begins with visually examining the mouth for symmetry, color, and size.
657
Breathing01:05

Breathing

The process of breathing, inhaling and exhaling, involves the coordinated movement of the chest wall, the lungs, and the muscles that move them. Two muscle groups with important roles in breathing are the diaphragm, located directly below the lungs, and the intercostal muscles, which lie between the ribs. When the diaphragm contracts, it moves downward, increasing the volume of the thoracic cavity and creating more room for the lungs to expand. When the intercostal muscles contract, the ribs...
61.6K