Gorlin-Goltz syndrome-a rare presentation

K. R. Bhat, C. K. Vasu, U. P. Rathnakar, G. Ravichandra, D. Acharya

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The Golin-Goltz syndrome is a rare, multisystemic and autosomal dominant disease. We are describing here, a case with an unusual presentation of purulent discharge into the mouth from infected cysts in the jaw, in a 22 year old male patient. The case was associated with some of the classical radiological features described in the literature for this syndrome.

Original languageEnglish
Pages (from-to)2899-2902
Number of pages4
JournalJournal of Clinical and Diagnostic Research
Volume4
Issue number4
Publication statusPublished - 06-10-2010
Externally publishedYes

Fingerprint

Focal Dermal Hypoplasia
Jaw Cysts
Basal Cell Nevus Syndrome
Mouth

All Science Journal Classification (ASJC) codes

  • Clinical Biochemistry

Cite this

Bhat, K. R., Vasu, C. K., Rathnakar, U. P., Ravichandra, G., & Acharya, D. (2010). Gorlin-Goltz syndrome-a rare presentation. Journal of Clinical and Diagnostic Research, 4(4), 2899-2902.
Bhat, K. R. ; Vasu, C. K. ; Rathnakar, U. P. ; Ravichandra, G. ; Acharya, D. / Gorlin-Goltz syndrome-a rare presentation. In: Journal of Clinical and Diagnostic Research. 2010 ; Vol. 4, No. 4. pp. 2899-2902.
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Bhat, KR, Vasu, CK, Rathnakar, UP, Ravichandra, G & Acharya, D 2010, 'Gorlin-Goltz syndrome-a rare presentation', Journal of Clinical and Diagnostic Research, vol. 4, no. 4, pp. 2899-2902.

Gorlin-Goltz syndrome-a rare presentation. / Bhat, K. R.; Vasu, C. K.; Rathnakar, U. P.; Ravichandra, G.; Acharya, D.

In: Journal of Clinical and Diagnostic Research, Vol. 4, No. 4, 06.10.2010, p. 2899-2902.

Research output: Contribution to journalArticle

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Bhat KR, Vasu CK, Rathnakar UP, Ravichandra G, Acharya D. Gorlin-Goltz syndrome-a rare presentation. Journal of Clinical and Diagnostic Research. 2010 Oct 6;4(4):2899-2902.