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Multiple hereditary osteochondromatosis: a case report.
Cigdem Küçükesmen1, Bugra Ozen, Mustafa Akçam
1Assistant Professor, Department of Pediatric Dentistry, Faculty of Dentistry, Suleyman Demirel University, Isparta, Turkey.
This case report details an 11-year-old boy with severe dental caries and growth retardation linked to Multiple Hereditary Osteochondromatosis (MHO) and frequent vomiting. Comprehensive dental treatment improved his oral health and nutrition.
Area of Science:
- Pediatric Dentistry
- Genetics
- Oral Health
Background:
- Multiple Hereditary Osteochondromatosis (MHO) is a rare genetic disorder.
- Vomiting, often a side effect of medications like Didronat, can lead to severe dental caries.
- Poor oral hygiene and malnutrition can exacerbate growth retardation in children.
Observation:
- An 11-year-old male patient diagnosed with MHO presented with severe dental caries, eating difficulties, and general growth retardation.
- The patient experienced frequent nausea and vomiting, contributing to poor oral hygiene and inadequate nutrition.
- Dental issues included extensive carious lesions and remaining roots, hindering chewing and eating.
Findings:
- Comprehensive dental interventions, including preventive, surgical, restorative, and prosthodontic treatments, were implemented.
- Nutritional counseling and oral hygiene reinforcement were key components of the management plan.
- The patient's oral health and nutritional status showed improvement following treatment.
Implications:
- This case highlights the critical link between systemic conditions, medication side effects, and oral health in pediatric patients.
- Early and integrated dental and medical management is crucial for children with MHO and associated complications.
- Addressing dental issues can significantly improve nutrition, growth, and overall quality of life in affected children.
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