Early diagnosis of Gorlin-Goltz syndrome: case report-Reference-Cited by-同舟云学术

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Early diagnosis of Gorlin-Goltz syndrome: case report

Published:2011-01-25 Issue:1 Volume:7 Page:
ISSN:1746-160X
Container-title:Head & Face Medicine
language:en
Short-container-title:Head Face Med

Author:

Casaroto Ana R,Rocha Loures Daniela CN,Moreschi Eduardo,Veltrini Vanessa C,Trento Cleverson L,Gottardo Vilmar D,Lara Vanessa S

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Dentistry,Otorhinolaryngology

Link

http://link.springer.com/article/10.1186/1746-160X-7-2/fulltext.html

Reference28 articles.

1. Yamamoto K, Yoshihashi H, Furuya N, Adachi M, Ito S, Tanaka Y, Masuno M, Chiyo H, Kurosawa K: Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: Report of two cases and review of the literature. Congenit Anom. 2009, 49: 8-14. 10.1111/j.1741-4520.2008.00212.x.

2. Gorlin RJ, Goltz RW: Multiple nevoid basal cell epithelioma, jaw cysts and bifid rib: A syndrome. New Engl J Med. 1960, 262: 908-12. 10.1056/NEJM196005052621803.

3. Cohen MM: Nevoid basal cell carcinoma syndrome: molecular biology and new hypotheses. Int J Oral Maxillofac Surg. 1999, 28: 216-23. 10.1034/j.1399-0020.1999.283280314.x.

4. Satinoff MI, Wells C: Multiple basal cell naevus syndrome in ancient. Egypt Med Hist. 1969, 13: 294-7.

5. Farndon PA, Del Mastro RG, Evans DG, Kilpatrick MW: Location of gene for Gorlin syndrome. Lancet. 1992, 339: 581-2. 10.1016/0140-6736(92)90868-4.

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