Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
Gorlin Goltz Syndrome: A Disease in Disguise
View through CrossRef
Gorlin Goltz syndrome also known as nevoid basal cell carcinoma is an autosomal dominant inherited disorder caused due to mutation in patched (PTCH) tumor suppressor gene present in the 9q chromosome. Gorlin goltz syndrome display diversified odontogenic as well as systemic manifestations. Early diagnosis and prompt treatment is mandatory to decrease morbidity and mortality. Here we present a subtle case report of a 17-year-old boy who presented with multiple odontogenic keratocysts of the mandible and maxilla which upon further examination was diagnosed as Gorlin Goltz Syndrome.
Auctores Publishing LLC
Title: Gorlin Goltz Syndrome: A Disease in Disguise
Description:
Gorlin Goltz syndrome also known as nevoid basal cell carcinoma is an autosomal dominant inherited disorder caused due to mutation in patched (PTCH) tumor suppressor gene present in the 9q chromosome.
Gorlin goltz syndrome display diversified odontogenic as well as systemic manifestations.
Early diagnosis and prompt treatment is mandatory to decrease morbidity and mortality.
Here we present a subtle case report of a 17-year-old boy who presented with multiple odontogenic keratocysts of the mandible and maxilla which upon further examination was diagnosed as Gorlin Goltz Syndrome.
Related Results
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
: Focal dermal hypoplasia, popularly known as the goltz syndrome, is an extremely rare multisystem disorder mainly involving the skin, skeletal system, and eyes. Being an X-linked ...
Gorlin–Goltz Syndrome with Eyelid Coloboma and Café au Lait Macule: Case Report and Literature Review
Gorlin–Goltz Syndrome with Eyelid Coloboma and Café au Lait Macule: Case Report and Literature Review
Gorlin–Goltz syndrome (GGS), also known as Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin syndrome, is a rare autosomal dominant inherited genodermatosis characterized by ...
GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW
GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW
Goltz Gorlin syndrome (GGS) is an multisystemic disease with an autosomal dominant disorder, with complete variance, though irregular cases have been described. This article includ...
An Update of Gorlin-Goltz Syndrome
An Update of Gorlin-Goltz Syndrome
Gorlin-Goltz syndrome encompasses a variety of clinical signs and symptoms including important oral manifestations which general dental practitioners should be aware of. In light o...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Abstract
Introduction
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease commonly affecting women of reproductive age. Its overlap with HELLP syndrome (Hemolysi...
Gorlin-Goltz Syndrome: A Case Report
Gorlin-Goltz Syndrome: A Case Report
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant inherited disorder; caused by mutations in the in the long
arm of chromosome 9 (q22.3-q31) and loss or mutations in the hed...
Case Report: Papillary thyroid carcinoma in Goltz–Gorlin syndrome
Case Report: Papillary thyroid carcinoma in Goltz–Gorlin syndrome
Goltz–Gorlin syndrome (GGS), also known as focal dermal hypoplasia, is a rare X-linked disorder caused by pathogenic variants in the PORCN gene and characterized by several abnorma...