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Autosomal recessive Robinow syndrome: a case report.
Ronald Grothe1, Cheryl Anderson-Cermin, Soraya Beiraghi
1Division of Pediatric Dentistry, Department of Developmental and Surgical Sciences, School of Dentistry, University of Minnesota, Minneapolis, Minn, USA.
Journal of Dentistry for Children (Chicago, Ill.)
|May 29, 2008
Summary
Recessive Robinow syndrome (RRS) is a rare genetic disorder affecting growth and facial features. This case study highlights how gingival hyperplasia in RRS can significantly impact tooth eruption and orthodontic treatment.
Area of Science:
- Genetics
- Pediatric Dentistry
- Oral Medicine
Background:
- Recessive Robinow syndrome (RRS) is an extremely rare genetic disorder characterized by short stature and distinctive facial, oral, and dental anomalies.
- Management of RRS necessitates a multidisciplinary approach involving dental and medical professionals.
Observation:
- This paper details the 4-year clinical and dental management of a female patient with RRS, from age 11 to 15.
- A key observation was the significant impediment to normal tooth eruption and orthodontic tooth movement caused by hyperplastic gingival tissues.
Findings:
- The patient's hyperplastic gingival tissues presented a substantial challenge for dental interventions.
- Effective management strategies were explored to overcome these gingival challenges.
Implications:
- This case underscores the critical role of specialized dental care in managing RRS.
- Understanding the impact of gingival hyperplasia is vital for successful orthodontic and restorative treatments in patients with RRS.
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