Literature DB >> 21806907

Case report: hypodontia and short roots in a child with Fraser syndrome.

E J Keene1, P F Day.   

Abstract

BACKGROUND: Fraser syndrome is a rare autosomal recessive disorder of which there has only previously been one case reported in the dental literature. The main characteristics are cryptophthalmos, syndactyly and genital abnormalities. Orofacial findings reported are: facial asymmetry, cleft lip and palate, high arched palate, dental crowding, fusion of primary teeth, dental hypoplasia, malocclusion, and supragingival calculus. CASE REPORT: A 15 year old girl with Fraser syndrome attended Bradford and Airedale salaried dental services complaining of painful mandibular anterior teeth. On examination she presented with hypodontia, shortened roots, and the mandibular anteriors had a titanium trauma splint fixed to reduce the mobility. This had been placed 4 years previously by a paediatric specialist. However oral hygiene was poor around it and therefore the patient had calculus and gingivitis. TREATMENT: The splint was removed followed by subgingival scaling under local analgesia, fissure sealants of all posterior teeth, regular oral hygiene instruction and scaling, and occasional use of chlorhexidine gel. FOLLOW-UP: She has been reviewed regularly with frequent scalings over two years.
CONCLUSION: This case reports the possibility of hypodontia and short roots being associated with Fraser syndrome.

Entities:  

Mesh:

Year:  2011        PMID: 21806907     DOI: 10.1007/bf03262810

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


  18 in total

Review 1.  Isolated and syndromic cryptophthalmos.

Authors:  I T Thomas; J L Frias; V Felix; L Sanchez de Leon; R A Hernandez; M C Jones
Journal:  Am J Med Genet       Date:  1986-09

Review 2.  The clinical spectrum of the Fraser syndrome: report of three new cases and review.

Authors:  J Gattuso; M A Patton; M Baraitser
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

3.  Fraser syndrome in a 96-year-old female.

Authors:  Mario Impallomeni; Deepak Subramanian; Nazim Mahmood; Joseph Illes; Illes Joseph
Journal:  Age Ageing       Date:  2006-11       Impact factor: 10.668

4.  Multiple congenital abnormalities associated with cryptophthalmia.

Authors:  C H Ide; P B Wollschlaeger
Journal:  Arch Ophthalmol       Date:  1969-05

Review 5.  Fraser syndrome.

Authors:  A Chattopadhyay; A S Kher; A D Udwadia; S V Sharma; B A Bharucha; A D Nicholson
Journal:  J Postgrad Med       Date:  1993 Oct-Dec       Impact factor: 1.476

6.  Fraser syndrome with renal agenesis in two consanguineous Turkish families.

Authors:  C Francannet; P Lefrançois; P Dechelotte; E Robert; G Malpuech; J M Robert
Journal:  Am J Med Genet       Date:  1990-08

7.  New observations on midline defects: coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders.

Authors:  J R Bierich; M Christie; J J Heinrich; A S Martinez
Journal:  Eur J Pediatr       Date:  1991-02       Impact factor: 3.183

8.  Clinical manifestations and oral findings in Fraser syndrome.

Authors:  Michele Baffi Diniz; Luciana Monti Lima; Nancy Tomoko Sacono; Andréia Bolzan de Paula; Lourdes dos Santos-Pinto
Journal:  J Dent Child (Chic)       Date:  2007 Sep-Dec

9.  Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.

Authors:  Lesley McGregor; Ville Makela; Susan M Darling; Sofia Vrontou; Georges Chalepakis; Catherine Roberts; Nicola Smart; Paul Rutland; Natalie Prescott; Jason Hopkins; Elizabeth Bentley; Alison Shaw; Emma Roberts; Robert Mueller; Shalini Jadeja; Nicole Philip; John Nelson; Christine Francannet; Antonio Perez-Aytes; Andre Megarbane; Bronwyn Kerr; Brandon Wainwright; Adrian S Woolf; Robin M Winter; Peter J Scambler
Journal:  Nat Genet       Date:  2003-06       Impact factor: 38.330

10.  Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli.

Authors:  Jolanta E Pitera; Peter J Scambler; Adrian S Woolf
Journal:  Hum Mol Genet       Date:  2008-09-11       Impact factor: 6.150

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