Hutchinson-Gilford progeria syndrome: Oral and craniofacial phenotypes

Oral Diseases

Volumn 15, Issue 3, 2009, Pages 187-195

  Domingo, D L ^a   Trujillo, M I ^a   Council, S E ^a   Merideth, M A ^b,c   Gordon, L B ^d   Wu, T ^a   Introne, W J ^b   Gahl, W A ^b   Hart, T C ^a  

^a NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

^d BROWN UNIVERSITY   (United States)

Author keywords

Craniofacial; Dentition; Oral; Phenotype; Progeria

Indexed keywords

ADOLESCENT; ANKYLOGLOSSIA; ARTICLE; CHILD; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; FEMALE; GENE MUTATION; HUMAN; HYPODONTIA; JAW MALFORMATION; MALE; MOUTH DISEASE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROGERIA; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; AGE DETERMINATION BY TEETH; ALVEOLAR PROCESS; ANODONTIA; CHILD; CHILD, PRESCHOOL; FACIES; FEMALE; HUMANS; INFANT; MALE; MALOCCLUSION; MAXILLOFACIAL ABNORMALITIES; MOUTH DISEASES; PHENOTYPE; PROGERIA; PROSPECTIVE STUDIES; SYNDROME; TOOTH ABNORMALITIES;

EID: 62749084955     PISSN: 1354523X     EISSN: 16010825     Source Type: Journal    
DOI: 10.1111/j.1601-0825.2009.01521.x     Document Type: Article

References (29)

1. Caldo-Teixeira AS, Puppin-Rontani RM (2003). Management of severe partial hypodontia: case report. J Clin Pediatr Dent 27 : 133 136.
2. Costaras-Volarich M, Pruzansky S (1984). Is the mandible intrinsically different in Apert and Crouzon syndromes? Am J Orthod 85 : 475 487.
3. Dharajani PJ (2002). Hypodontia: etiology, clinical features, and management. Quintessence Int 33 : 294 302.
4. Fong LG, Ng JK, Meta M et al (2004). Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice. Proc Natl Acad Sci U S A 101 : 18111 18116.
5. Goldman RD, Shumaker DK, Erdos MR et al (2004). Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci U S A 101 : 8963 8968.
6. Gordon LB, McCarten KM, Giobbie-Hurder A et al (2007). Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development. Pediatrics 120 : 824 833.
7. Hagg U, Taranger J (1985). Dental development, dental age and tooth counts. Angle Orthod 55 : 93 107.
8. Hasty MF, Vann WF (1988). Progeria in a pediatric dental patient: literature review and case report. Pediatr Dent 10 : 314 319.
9. Hennekam RC (2006). Hutchinson-Gilford progeria syndrome: review of the phenotype. Am J Med Genet A 140A : 2603 2624.
10. Martin GM (2005). Genetic modulation of senescent phenotypes in Homo sapiens. Cell 120 : 523 532.
11. Mau U, Kendziorra H, Kaiser P (1997). Restrictive dermopathy: report and review. Am J Med Genet 71 : 179 185.
12. McClintock D, Ratner D, Lokuge M et al (2007). The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin. PLoS ONE 2 : e1269.
13. Merideth MA, Gordon LB, Clauss S et al (2008). Phenotype and course of Hutchinson-Gilford progeria syndrome. N Engl J Med 358 : 592 604.
14. Neville BW, Damm DD, Allen CM, Bouquot JE, eds (2002a). Developmental defects of the oral and maxillofacial region. Oral & maxillofacial pathology. 2nd edn. WB Saunders Co. : Philadelphia, pp. 1 48.
15. Neville BW, Damm DD, Allen CM, Bouquot JE, eds (2002b). Abnormalities of teeth. Oral & maxillofacial pathology. 2nd edn. WB Saunders Co. : Philadelphia, pp. 49 106.
16. Neville BW, Damm DD, White DK (2003). Dentinogenesis imperfecta (hereditary opalescent dentin, capdepont teeth). In : Neville BW, Damm DD, Allen CM, Bouquot JE, eds. Color atlas of clinical oral pathology. 2nd edn. BC Decker Inc. : Hamilton, ON, pp. 49 106.
17. Nunn JH, Carter NE, Gillgrass TJ et al (2003). The interdisciplinary management of hypodontia: background and role of paediatric dentistry. Br Dent J 194 : 245 251.
18. Paradisi M, McClintock D, Boguslavsky RL et al (2005). Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress. BMC Cell Biol 6 : 27.
19. Pollex RL, Hegele RA (2004). Hutchinson-Gilford progeria syndrome. Clin Genet 66 : 375 381.
20. Ruffoli R, Giambelluca MA, Scavuzzo MC et al (2005). Ankyloglossia: a morphofunctional investigation in children. Oral Dis 11 : 170 174.
21. Sarkar PK, Shinton RA (2001). Hutchinson-Guilford progeria syndrome. Postgrad Med J 77 : 312 317.
22. Stephen A, Cengiz SB (2003). The use of overdentures in the management of severe hypodontia associated with microdontia: a case report. J Clin Pediatr Dent 27 : 219 222.
23. Uhrhammer NA, Lafarge L, Dos Santos L et al (2006). Werner syndrome and mutations of the WRN and LMNA genes in France. Hum Mutat 27 : 718 719.
24. Wesley RK, Delaney JR, Litt R (1979). Progeria: clinical consideration of an isolated case. J Dent Child 46 : 487 492.
25. White SC, Pharoah MJ (2000). Radiographic interpretation of pathology. In : White SC, Pharoah MJ, eds. Oral radiology principles and interpretation. 4th edn. Mosby Inc. : St. Louis, MO, pp. 319 320.
26. Woelfel JB, ed (1990a). Terminology. Dental anatomy: its relevance to dentistry. 4th edn. Lea & Febiger : Philadelphia, PA, pp. 18 32.
27. Woelfel JB, ed (1990b). Permanent mandibular molars. Dental anatomy: its relevance to dentistry. 4th edn. Lea & Febiger : Philadelphia, PA, pp. 155 180.
28. Yu QX, Zeng LH (1991). Progeria; report of a case and review of the literature. J Oral Pathol Med 20 : 86 88.
29. Zhu JF, Marcushamer M, King DL, Henry RJ (1996). Supernumerary and congenitally absent teeth: a literature review. J Clin Pediatr Dent 20 : 87 95.