Literature DB >> 24327104

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

M Gendronneau1, O Kérourédan, S Taque, J L Sixou, M Bonnaure-Mallet.   

Abstract

BACKGROUND: Schimke immuno-osseous dysplasia (SIOD) is a rare, severe, autosomal recessive disorder that results in spondyloepiphyseal dysplasia, renal dysfunction, immunodeficiency, facial dysmorphism and growth failure. Little is known about oral features associated with SIOD. Some of the dental anomalies encountered are specific to SIOD and have only been reported in individuals with SIOD. CASE REPORT: This paper describes the clinical and radiographic dental manifestations of SIOD in two Caucasian brothers. Both lived to be about 10 years old. After a variety of symptoms were reported, a diagnosis of SIOD was finally made when the brothers were, respectively, 5 and 8 years old. At that time, dental anomalies, such as dyschromia, bulbous crowns, short and thin roots, had not been taken into account to establish the diagnosis. However, knowledge of the dental features characteristic of this disease could have helped make the diagnosis. Although both were caries- and periodontal disease-free, special attention was focused on prevention, including dietary counselling, plaque control, oral hygiene instructions and the use of fluoridated toothpaste. FOLLOW-UP: The two patients were followed every 6 months, for over 2 years (until their death), by both a private dentist and a university hospital dentist, which helped them maintain good oral health. Oral hygiene was assessed at each appointment and fissure sealants were placed by the private practitioner on their first permanent molars.
CONCLUSION: This report describes dental anomalies specific to SIOD that could facilitate diagnosis. Clinicians and dentists should work in collaboration to diagnose and treat children with SIOD. These patients require regular and specific dental management because of their fragile health and their characteristic dental anomalies. Ideally, preventive visits should be scheduled every 6 months in addition to curative visits as needed.

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Year:  2013        PMID: 24327104      PMCID: PMC5127816          DOI: 10.1007/s40368-013-0099-3

Source DB:  PubMed          Journal:  Eur Arch Paediatr Dent        ISSN: 1818-6300


  12 in total

1.  Longevity in Schimke immuno-osseous dysplasia.

Authors:  S Lou; P Lamfers; N McGuire; C F Boerkoel
Journal:  J Med Genet       Date:  2002-12       Impact factor: 6.318

2.  Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature.

Authors:  C F Boerkoel; S O'Neill; J L André; P J Benke; R Bogdanovíć; M Bulla; A Burguet; S Cockfield; I Cordeiro; J H Ehrich; S Fründ; D F Geary; A Ieshima; F Illies; M W Joseph; I Kaitila; G Lama; B Leheup; M D Ludman; D R McLeod; A Medeira; D V Milford; T Ormälä; Z Rener-Primec; A Santava; H G Santos; B Schmidt; G C Smith; J Spranger; N Zupancic; R Weksberg
Journal:  Eur J Pediatr       Date:  2000 Jan-Feb       Impact factor: 3.183

3.  Schimke immuno-osseous dysplasia: a cell autonomous disorder?

Authors:  Leah I Elizondo; Cheng Huang; Jennifer L Northrop; Kimiko Deguchi; Johanna M Clewing; Dawna L Armstrong; Cornelius F Boerkoel
Journal:  Am J Med Genet A       Date:  2006-02-15       Impact factor: 2.802

4.  Clinical quiz. Schimke immunoosseous dysplasia syndrome (SIOD).

Authors:  F Rodrigo; J Ferrer-Cañabate; S Gracia; I Tovar; E Borrajo; C Tellez; P Martínez
Journal:  Pediatr Nephrol       Date:  2001-07       Impact factor: 3.714

5.  Dental findings in the Schimke immuno-osseous dysplasia.

Authors:  M A da Fonseca
Journal:  Am J Med Genet       Date:  2000-07-17

Review 6.  Juvenile variant of Schimke immunoosseous dysplasia.

Authors:  K Hashimoto; A Takeuchi; A Ieshima; M Takada; M Kasagi
Journal:  Am J Med Genet       Date:  1994-02-01

7.  Generalized atherosclerosis sparing the transplanted kidney in Schimke disease.

Authors:  Thomas Lücke; Katja M Marwedel; Nele K Kanzelmeyer; Akira Hori; Gisela Offner; Hans-Heinrich Kreipe; Jochen H H Ehrich; Anibh M Das
Journal:  Pediatr Nephrol       Date:  2004-03-31       Impact factor: 3.714

Review 8.  Schimke immuno-osseous dysplasia: case report and review.

Authors:  M D Ludman; D E Cole; J F Crocker; M M Cohen
Journal:  Am J Med Genet       Date:  1993-10-01

9.  HARP is an ATP-driven annealing helicase.

Authors:  Timur Yusufzai; James T Kadonaga
Journal:  Science       Date:  2008-10-31       Impact factor: 47.728

10.  The annealing helicase HARP protects stalled replication forks.

Authors:  Jingsong Yuan; Gargi Ghosal; Junjie Chen
Journal:  Genes Dev       Date:  2009-09-30       Impact factor: 11.361

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  2 in total

Review 1.  Periodontal and other oral manifestations of immunodeficiency diseases.

Authors:  M E Peacock; R M Arce; C W Cutler
Journal:  Oral Dis       Date:  2016-10-10       Impact factor: 3.511

2.  Dental abnormalities in individuals with pathogenic germline variation in DICER1.

Authors:  Sooji Choi; Janice S Lee; Carol W Bassim; Harvey Kushner; Ann G Carr; Pamela J Gardner; Laura A Harney; Kris Ann P Schultz; Douglas R Stewart
Journal:  Am J Med Genet A       Date:  2019-07-16       Impact factor: 2.802

  2 in total

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