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Bimaxillary concomitant hypohyperdontia in a 10-year-old child
Pratik B Kariya1, Sweta Singh2, Narayan Kulkarni3
1Department of Pedodontics and Preventive Dentistry, KM Shah Dental College and Hospital, Sumandeep Vidyapeeth, Vadodara, Gujarat, India.
This case report details a rare instance of concomitant hypohyperdontia (CHH), where a patient exhibited both tooth agenesis (hypodontia) and supernumerary teeth (hyperdontia) simultaneously. This rare dental anomaly affects both jaws, presenting unique diagnostic and treatment challenges.
Area of Science:
- Dentistry
- Human Genetics
- Oral Pathology
Background:
- Numerical anomalies like hypodontia (missing teeth) and hyperdontia (extra teeth) are common in human dentition.
- Simultaneous occurrence of both hypodontia and hyperdontia in a single individual, termed concomitant hypohyperdontia (CHH), is exceptionally rare.
- The etiology of CHH remains largely unknown, with reported prevalence ranging from 0.002% to 3.1%.
Observation:
- This case report presents a rare instance of bimaxillary concomitant hypohyperdontia.
- The observed case involved the absence of both mandibular central incisors (hypodontia).
- Concurrently, two supernumerary teeth were present in the maxillary anterior segment (hyperdontia).
Findings:
- The study documents a unique presentation of CHH affecting both the maxilla and mandible.
- This specific case demonstrates a combination of missing mandibular incisors and supernumerary maxillary incisors.
- The bimaxillary nature of this CHH presentation is particularly noteworthy.
Implications:
- This case underscores the importance of recognizing rare dental anomalies for accurate diagnosis and treatment planning.
- Further research into the genetic and developmental factors underlying CHH is warranted.
- Reporting such rare cases contributes valuable data to understanding the spectrum of human dental anomalies.
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