Literature DB >> 3970117

Oculocerebrocutaneous syndrome.

R D Wilson, L Traverse, J G Hall, C O Flodmark, J Rootman.   

Abstract

A female infant was found at birth to have an oculocerebrocutaneous syndrome in which the main clinical features include orbital cyst, cerebral malformations, accessory skin tags, and focal hypoplasia or "punched-out" skin lesions. This case, like the four previously reported, was sporadic.

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Year:  1985        PMID: 3970117     DOI: 10.1016/0002-9394(85)90222-3

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  5 in total

Review 1.  Oculocerebrocutaneous syndrome.

Authors:  L M Bleeker-Wagemakers; B C Hamel; R C Hennekam; F A Beemer; H W Oorthuys
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318

2.  The oculocerebrocutaneous (Delleman) syndrome.

Authors:  L I al-Gazali; D Donnai; S A Berry; B Say; R F Mueller
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

3.  Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.

Authors:  U Moog; M C Jones; L M Bird; W B Dobyns
Journal:  J Med Genet       Date:  2005-05-06       Impact factor: 6.318

4.  Delleman syndrome: a case report and review.

Authors:  R De Cock; A Merizian
Journal:  Br J Ophthalmol       Date:  1992-02       Impact factor: 4.638

5.  Delleman Oorthuys syndrome: 'Oculocerebrocutaneous syndrome'.

Authors:  Vipul Arora; Usha R Kim; Hadi M Khazei
Journal:  Indian J Ophthalmol       Date:  2009 Sep-Oct       Impact factor: 1.848

  5 in total

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