Literature DB >> 2160065

The Gorlin-Goltz syndrome: case report.

G Manzi1, A Magli, B Pignalosa, G Liguori.   

Abstract

Focal dermal hypoplasia is a syndrome characterized by anomalies of cutaneous, osseous, dental and ocular structures. Because of the ocular anomalies, this syndrome should be regarded as a fifth type of phakomatosis. The differences between the fibroblasts obtained from skin lesions and fibroblasts obtained from normal skin and controls could be the demonstration of mosaicism and the consequence of lyonization. The authors present the case of a baby with typical anomalies of the Gorlin-Goltz syndrome and abnormal growth characteristics of skin fibroblasts.

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Year:  1990        PMID: 2160065     DOI: 10.1159/000310086

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN: 0030-3755            Impact factor:   3.250


  5 in total

1.  Anterior segment dysgenesis in mosaic Turner syndrome.

Authors:  I C Lloyd; P M Haigh; J Clayton-Smith; P Clayton; D A Price; A E Ridgway; D Donnai
Journal:  Br J Ophthalmol       Date:  1997-08       Impact factor: 4.638

2.  Focal dermal hypoplasia: A novel finding in disguise.

Authors:  S Nathwani; K Martin; R Bunyan
Journal:  J Oral Biol Craniofac Res       Date:  2018-02-01

3.  Nevoid-basal cell carcinoma syndrome: a case report and overview on diagnosis and management.

Authors:  Shridhar D Baliga; Sanjay S Rao
Journal:  J Maxillofac Oral Surg       Date:  2010-06-04

4.  Choroidal coloboma in a case of tay-sachs disease.

Authors:  Nasreen Raees Ahmed; Koushik Tripathy; Vivek Kumar; Varun Gogia
Journal:  Case Rep Ophthalmol Med       Date:  2014-09-10

5.  Histogenesis of retinal dysplasia in trisomy 13.

Authors:  Ada Chan; Satyan Lakshminrusimha; Reid Heffner; Federico Gonzalez-Fernandez
Journal:  Diagn Pathol       Date:  2007-12-18       Impact factor: 2.644

  5 in total

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