A case of Beckwith-Wiedemann syndrome with peculiar dental findings

M Callea; Izzet Yavuz; G Clarich; A. Gunay; A Vinciguerra; Mehmet Unal; C. Sahbaz; M. Sinan Dogan; Francisco Cammarata-Scalisi

A case of Beckwith-Wiedemann syndrome with peculiar dental findings

M Callea, Izzet Yavuz, G Clarich, A. Gunay, A Vinciguerra, Mehmet Unal, C. Sahbaz, M. Sinan Dogan, Francisco Cammarata-Scalisi

Research output: Contribution to journal › Article › peer-review

Abstract

BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been reported so far.

CASE REPORT: We report on a case of BWS, describing all features expanding the knowledge on oro-dento-facial phenotypes, along with a review of the literature.

Original language	English
Pages (from-to)	315-317
Number of pages	3
Journal	European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry
Volume	17
Issue number	4
Publication status	Published - Dec 2016

Keywords

Journal Article

Cite this

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title = "A case of Beckwith-Wiedemann syndrome with peculiar dental findings",

abstract = "BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been reported so far.CASE REPORT: We report on a case of BWS, describing all features expanding the knowledge on oro-dento-facial phenotypes, along with a review of the literature.",

keywords = "Journal Article",

author = "M Callea and Izzet Yavuz and G Clarich and A. Gunay and A Vinciguerra and Mehmet Unal and C. Sahbaz and {Sinan Dogan}, M. and Francisco Cammarata-Scalisi",

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T1 - A case of Beckwith-Wiedemann syndrome with peculiar dental findings

AU - Callea, M

AU - Yavuz, Izzet

AU - Clarich, G

AU - Gunay, A.

AU - Vinciguerra, A

AU - Unal, Mehmet

AU - Sahbaz, C.

AU - Sinan Dogan, M.

AU - Cammarata-Scalisi, Francisco

PY - 2016/12

Y1 - 2016/12

N2 - BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been reported so far.CASE REPORT: We report on a case of BWS, describing all features expanding the knowledge on oro-dento-facial phenotypes, along with a review of the literature.

AB - BACKGROUND: Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been reported so far.CASE REPORT: We report on a case of BWS, describing all features expanding the knowledge on oro-dento-facial phenotypes, along with a review of the literature.

KW - Journal Article

M3 - Article

C2 - 28045321

SN - 1591-996X

VL - 17

SP - 315

EP - 317

JO - European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry

JF - European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry

IS - 4

ER -

A case of Beckwith-Wiedemann syndrome with peculiar dental findings

Abstract

Keywords

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