Dental abnormalities and preventive oral care in Schimke immuno-osseous dysplasia

Gendronneau, Marion; Kérourédan, Olivia; Taque, Sophie; Sixou, Jean-Louis; Bonnaure‐Mallet, Martine

doi:10.1007/s40368-013-0099-3

Cited by 7 publications

(5 citation statements)

References 12 publications

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“…Oral manifestations-Dental anomalies reported include microdontia, hypodontia, short and thin tooth roots, and malformed primary and/or permanent molars (Morimoto et al, 2012;Gendronneau et al, 2014). Morimoto et al were the first to scientifically investigate the oral defects associated with SIOD (Morimoto et al, 2012).…”

Section: Treatment-optimal Treatment For Patients With Dkc Is Hct Fromentioning

confidence: 99%

Periodontal and other oral manifestations of immunodeficiency diseases

2016

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The list of immunodeficiency diseases grows each year as novel disorders are discovered, classified, and sometimes reclassified due to our ever-increasing knowledge of immune system function. Although the number of patients with secondary immunodeficiencies (SIDs) greatly exceeds those with primary immunodeficiencies (PIDs), the prevalence of both appears to be on the rise probably because of scientific breakthroughs that facilitate earlier and more accurate diagnosis. Primary immunodeficiencies in adults are not as rare as once thought. Globally, the main causes of secondary immunodeficiency are HIV infection and nutritional insufficiencies. Persons with acquired immune disorders such as AIDS caused by the Human Immunodeficiency Virus (HIV) are now living long and fulfilling lives as a result of highly active antiretroviral therapy (HAART). Irrespective of whether the patient’s immune deficient state is a consequence of a genetic defect or is secondary in nature, dental and medical practitioners must be aware of the constant potential for infections and/or expressions of autoimmunity in these individuals. The purpose of this paper is to review the most common conditions resulting from primary and secondary immunodeficiency states, how they are classified, and the detrimental manifestations of these disorders on the periodontal and oral tissues.

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Section: Treatment-optimal Treatment For Patients With Dkc Is Hct Fromentioning

confidence: 99%

Periodontal and other oral manifestations of immunodeficiency diseases

2016

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“…Short roots have also been encountered in short stature patients [22,23] and short stature conditions [24,25]. Short roots of multiple teeth have also been reported in patients with Turner syndrome [26,27], Frazer syndrome [28], Stevens-Johnson syndrome [29][30][31][32][33], Hallerman-Streiff syndrome [34], and Schimcke immuno-osseous dysplasia [35]. Some metabolic disorders like hypophospatasia [36], pseudohypoparathyroidism [37,38], and vitamin D-dependent rickets, type I [39] have also been associated with short roots.…”

Section: Discussionmentioning

confidence: 99%

Presentation of a Case of Short Root Anomaly in an 11-Year-Old Child

Trimeridou

Arhakis

Arapostathis

2023

Case Reports in Dentistry

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Short root anomaly (SRA) is a developmental anomaly in which the affected teeth present morphologically normal crowns and short, round roots. The exact cause of SRA is unknown. A case of an 11-year-old female patient with SRA is described. The patient presented short, round roots of all permanent teeth but first molars. Maxillary lateral incisors presented severe root resorption and mobility. Treatment plan included preservation of the maxillary lateral incisors by splinting them to their adjacent teeth using a stainless steel coaxial wire. A custom mouthguard for dental trauma protection was also constructed using a computer-aided design - computer-aided manufacturing (CAD–CAM) system in order to fabricate 3D-printed dental casts. At 2-year follow-up, the mobility of maxillary lateral incisors decreased, and the patient’s dentition remained stable. Considerations regarding differential diagnosis, orthodontic management, and treatment options after an eventual loss of teeth are thoroughly discussed.

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“…Clinically, our observations may be useful in the recognition of DICER1 ‐carriers. Bulbous crowns (with thin roots) can be diagnostically useful in Schimke immunoosseous dysplasia, a rare disorder of short stature, nephropathy and T‐cell deficiency (Gendronneau, Kerouredan, Taque, Sixou, & Bonnaure‐Mallet, ; Morimoto et al, ). In the general population, the frequency of periodontal disease is approximately 8.5% (age 20–64 years; US National Health and Nutrition Examination Survey, 1999–2004), taurodontism is 2.5% (Jaspers & Witkop Jr., ) and that of bulbousness is unknown.…”

Section: Discussionmentioning

confidence: 99%