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

Goltz-Gorlin syndrome: A rare genodermatosis


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
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2319-7250.143673

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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.


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