Indian Journal of Paediatric Dermatology

CASE REPORT
Year
: 2014  |  Volume : 15  |  Issue : 3  |  Page : 133--136

Goltz-Gorlin syndrome: A rare genodermatosis


Dimple Kothari, Chitra S Nayak, Bhushan Madke, Atul Giri 
 Department of Dermatology, T.N. Medical College and BYL Nair Hospital, Mumbai, Maharashtra, India

Correspondence Address:
Chitra S Nayak
Department of Dermatology, T.N. Medical College and BYL Nair Hospital, Mumbai - 400 008, Maharashtra
India

We report a case of a 6-year-old girl with typical anomalies of Goltz syndrome characterized by linear and reticulate atrophy of the skin, significant defects of the skeleton, dental structures, eyes, and soft tissues. No family member had such features. A brief overview of the syndrome is presented in an attempt to incorporate associated anomalies reported so far.


How to cite this article:
Kothari D, Nayak CS, Madke B, Giri A. Goltz-Gorlin syndrome: A rare genodermatosis.Indian J Paediatr Dermatol 2014;15:133-136


How to cite this URL:
Kothari D, Nayak CS, Madke B, Giri A. Goltz-Gorlin syndrome: A rare genodermatosis. Indian J Paediatr Dermatol [serial online] 2014 [cited 2020 Oct 21 ];15:133-136
Available from: https://www.ijpd.in/article.asp?issn=2319-7250;year=2014;volume=15;issue=3;spage=133;epage=136;aulast=Kothari;type=0