Hemifacial Microsomia, though challenging, offers hope for enhanced facial symmetry and function through advanced surgical interventions, providing individuals with improved confidence and quality of life.
Causes and Associated Factors
The exact cause of hemifacial microsomia remains largely unknown, although genetic and environmental factors may contribute to its development. This condition often presents various associated problems, including jaw deformities, ear anomalies, facial nerve weakness, eye abnormalities, and other congenital malformations. Children with hemifacial microsomia may experience various associated problems, with the severity of visible deformity varying from subtle to extreme. The most common manifestation is a small lower jaw with a shifted chin point, which can lead to bite irregularities or malocclusion. External ear involvement is common, with the potential for microtia or anotia (underdeveloped or absent ear), skin tags, and sinus pits around the ear. Facial nerve involvement may result in one-sided facial weakness or paralysis, while cheekbone deficiency and downward displacement of the outer eye corner are also observed. Other congenital deformities may coexist with hemifacial microsomia, affecting various organ systems such as the spine, gastrointestinal tract, heart, kidneys, and lungs. While certain syndromes like Goldenhar and Treacher Collins may feature hemifacial microsomia characteristics, most cases occur as isolated occurrences within families, suggesting a multifactorial inheritance pattern.