Literature DB >> 18446333

Craniofacial and temporal bone CT findings in cleidocranial dysplasia.

Guido E Gonzalez1, Paul A Caruso, Juan E Small, Robert W Jyung, Maria J Troulis, Hugh D Curtin.   

Abstract

Cleidocranial dysplasia (CCD) is a multistructural polyostotic genetic disorder that results from mutation of the CBFA1 gene. Hearing loss is a frequent finding in CCD. We describe the CT craniofacial findings in CCD and provide a comprehensive discussion of the CT temporal bone findings in these patients.

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Mesh：

Year:  2008        PMID： 18446333     DOI： 10.1007/s00247-008-0866-1

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  7 in total

Review 1.  Cleidocranial dysplasia - review with an emphasis on otological and audiological manifestations.

Authors:  Nili Segal; Moshe Puterman
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2007-01-18       Impact factor: 1.675

2.  Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.

Authors:  S Mundlos; F Otto; C Mundlos; J B Mulliken; A S Aylsworth; S Albright; D Lindhout; W G Cole; W Henn; J H Knoll; M J Owen; R Mertelsmann; B U Zabel; B R Olsen
Journal:  Cell       Date:  1997-05-30       Impact factor: 41.582

3.  Congenital anomalies of the middle ear: presentation of two cases.

Authors:  J W Pou
Journal:  Laryngoscope       Date:  1971-06       Impact factor: 3.325

4.  A natural history of cleidocranial dysplasia.

Authors:  S C Cooper; C M Flaitz; D A Johnston; B Lee; J T Hecht
Journal:  Am J Med Genet       Date:  2001-11-15

Review 5.  Hearing loss as a presenting symptom of cleidocranial dysplasia.

Authors:  I Dhooge; B Lantsoght; M Lemmerling; B Vanzieleghem; G Mortier
Journal:  Otol Neurotol       Date:  2001-11       Impact factor: 2.311

6.  Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.

Authors:  Ann Marie B Visosky; Jacob Johnson; Becky Bingea; Theresa Gurney; Anil K Lalwani
Journal:  Laryngoscope       Date:  2003-09       Impact factor: 3.325

Review 7.  Dentomaxillofacial variability of cleidocranial dysplasia: clinicoradiological presentation and systematic review.

Authors:  I Golan; U Baumert; B P Hrala; D Müssig
Journal:  Dentomaxillofac Radiol       Date:  2003-11       Impact factor: 2.419
  7 in total
  4 in total

Review 1.  First and second branchial arch syndromes: multimodality approach.

Authors:  Elodie Senggen; Tarek Laswed; Jean-Yves Meuwly; Leonor Alamo Maestre; Bertrand Jaques; Reto Meuli; François Gudinchet
Journal:  Pediatr Radiol       Date:  2010-10-06

2.  A novel gene mutation of Runx2 in cleidocranial dysplasia.

Authors:  You-Jian Peng; Qiao-Yun Chen; Dong-Jie Fu; Zhi-Ming Liu; Tian-Tian Mao; Jun Li; Wen-Ting She
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2017-10-20

Review 3.  Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family.

Authors:  A Impellizzeri; G Midulla; U Romeo; C La Monaca; E Barbato; G Galluccio
Journal:  Int J Dent       Date:  2018-07-04

4.  Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.

Authors:  Alessio Danilo Inchingolo; Assunta Patano; Giovanni Coloccia; Sabino Ceci; Angelo Michele Inchingolo; Grazia Marinelli; Giuseppina Malcangi; Valentina Montenegro; Claudia Laudadio; Giulia Palmieri; Ioana Roxana Bordea; Emanuela Ponzi; Paola Orsini; Romina Ficarella; Antonio Scarano; Felice Lorusso; Gianna Dipalma; Massimo Corsalini; Mattia Gentile; Daniela Di Venere; Francesco Inchingolo
Journal:  Medicina (Kaunas)       Date:  2021-12-10       Impact factor: 2.430
  4 in total

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