Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review
Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review
About this item
Full title
Author / Creator
Lavrysen, Emilie , Loeys, Bart , Vanderveken, Olivier M. , Boudewyns, An , Department of Medical Genetics, Antwerp University Hospital, Edegem, Belgium , Department of Otorhinolaryngology and Head & Neck Surgery, Antwerp University Hospital, Edegem, Belgium, Faculty of Medicine and Translational Neurosciences, University of Antwerp, Antwerp, Belgium and Department of Otorhinolaryngology and Head & Neck Surgery, Antwerp University Hospital, Edegem, Belgium
Publisher
AVES
Journal title
Language
English
Formats
Publication information
Publisher
AVES
Subjects
More information
Scope and Contents
Contents
Goltz-Gorlin syndrome, also known as focal dermal hypoplasia or nevoid basal cell carcinoma syndrome, is a rare multisystemic disease caused by autosomal dominant mutations in the PORCN gene. The characterizing features are keratocystic odontogenic tumors in the jaw, multiple basal cell carcinomas, calcification of the falx cerebri, palmar or plant...
Alternative Titles
Full title
Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review
Authors, Artists and Contributors
Author / Creator
Loeys, Bart
Vanderveken, Olivier M.
Boudewyns, An
Department of Medical Genetics, Antwerp University Hospital, Edegem, Belgium
Department of Otorhinolaryngology and Head & Neck Surgery, Antwerp University Hospital, Edegem, Belgium, Faculty of Medicine and Translational Neurosciences, University of Antwerp, Antwerp, Belgium
Department of Otorhinolaryngology and Head & Neck Surgery, Antwerp University Hospital, Edegem, Belgium
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_5b9e0551e6994684b4d80565b5cd2103
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5b9e0551e6994684b4d80565b5cd2103
Other Identifiers
ISSN
2684-4907
E-ISSN
2684-4907
DOI
10.5152/B-ENT.2022.21817
