Cargando…

Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature

Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with several neurological, cutaneous and skeletal manifestations. Epilepsy has been previously reported as a finding in Gorlin–Goltz syndrome but remains ill-described in the context of this disease. We...

Descripción completa

Detalles Bibliográficos
Autores principales: Tomasso, Daniel, Assi, Elie Bou, Nguyen, Dang Khoa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560589/
https://www.ncbi.nlm.nih.gov/pubmed/33089135
http://dx.doi.org/10.1016/j.ebr.2020.100384
_version_ 1783595117837287424
author Tomasso, Daniel
Assi, Elie Bou
Nguyen, Dang Khoa
author_facet Tomasso, Daniel
Assi, Elie Bou
Nguyen, Dang Khoa
author_sort Tomasso, Daniel
collection PubMed
description Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with several neurological, cutaneous and skeletal manifestations. Epilepsy has been previously reported as a finding in Gorlin–Goltz syndrome but remains ill-described in the context of this disease. We report two new patients with Gorlin–Goltz syndrome featuring epilepsy and review the existing literature on the topic.
format Online
Article
Text
id pubmed-7560589
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-75605892020-10-20 Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature Tomasso, Daniel Assi, Elie Bou Nguyen, Dang Khoa Epilepsy Behav Rep Case Report Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with several neurological, cutaneous and skeletal manifestations. Epilepsy has been previously reported as a finding in Gorlin–Goltz syndrome but remains ill-described in the context of this disease. We report two new patients with Gorlin–Goltz syndrome featuring epilepsy and review the existing literature on the topic. Elsevier 2020-08-07 /pmc/articles/PMC7560589/ /pubmed/33089135 http://dx.doi.org/10.1016/j.ebr.2020.100384 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Tomasso, Daniel
Assi, Elie Bou
Nguyen, Dang Khoa
Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title_full Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title_fullStr Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title_full_unstemmed Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title_short Gorlin–Goltz syndrome and epilepsy: A two-case report and review of the literature
title_sort gorlin–goltz syndrome and epilepsy: a two-case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560589/
https://www.ncbi.nlm.nih.gov/pubmed/33089135
http://dx.doi.org/10.1016/j.ebr.2020.100384
work_keys_str_mv AT tomassodaniel gorlingoltzsyndromeandepilepsyatwocasereportandreviewoftheliterature
AT assieliebou gorlingoltzsyndromeandepilepsyatwocasereportandreviewoftheliterature
AT nguyendangkhoa gorlingoltzsyndromeandepilepsyatwocasereportandreviewoftheliterature