Literature DB >> 3935793

Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

M A Patton, K M Laurence.   

Abstract

Three new cases of oculodentodigital (ODD) syndrome are reported. The clinical features are discussed and the development of the characteristic facial appearance is illustrated. Conductive deafness is reported in one of our cases and has been reported in six previous cases. It is suggested that it is a feature of the syndrome which is amenable to treatment.

Entities:  

Mesh：

Year:  1985        PMID： 3935793      PMCID： PMC1049484          DOI： 10.1136/jmg.22.5.386

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  10 in total

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Authors:  G J Kurlander; N W Lavy; J A Campbell
Journal:  Radiology       Date:  1966-01       Impact factor: 11.105

6.  Orodigitofacial dysostosis and oculodentodigital dysplasia. Two distinct syndromes with some similarities.

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Journal:  Oral Surg Oral Med Oral Pathol       Date:  1967-03

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Journal:  Am J Med Genet       Date:  1981

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Authors:  G F Judisch; A Martin-Casals; J W Hanson; W H Olin
Journal:  Arch Ophthalmol       Date:  1979-05

10.  Oculodentodigital dysplasia syndrome. Report of four cases.

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Journal:  Acta Paediatr Scand       Date:  1977-09
  10 in total
  6 in total

Review 1.  International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone.

Authors:  J Spranger
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

2.  Oculodental digital dysplasia: neuroimaging in a kindred.

Authors:  L E Ginsberg; T Jewett; R Grub; W T McLean
Journal:  Neuroradiology       Date:  1996-01       Impact factor: 2.804

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Journal:  Br J Ophthalmol       Date:  1998-03       Impact factor: 4.638

Review 4.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

5.  Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

Authors:  L A Brueton; S M Huson; B Farren; R M Winter
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

6.  Novel mutations in GJA1 cause oculodentodigital syndrome.

Authors:  A Fenwick; R J Richardson; J Butterworth; M J Barron; M J Dixon
Journal:  J Dent Res       Date:  2008-11       Impact factor: 6.116
  6 in total

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