Results 71 to 80 of about 5,083 (170)

Gorlin-Goltz Syndrome: Case Report of a Rare Hereditary Disorder

Case Reports in Dentistry, 2012
Introduction. Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. Case Report.
Ashutosh Agrawal, Aditi Murari, Sunil Vutukuri, Arun Singh   +3 more
doaj   +1 more source

Jaw cyst-Basal cell nevus-Bifid rib syndrome: A case report

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2007
Jaw cyst-Basal cell nevus-Bifid rib syndrome or Gorlin-Goltz syndrome involves multiple organ system. The most common findings include multiple odontogenic keratocysts in the jaws and basal cell nevus on the skin that have an early age onset.
Rai S, Gauba K
doaj  

Prenatal detection of Gorlin–Goltz syndrome: a case report and focused review of the literature

Frontiers in Medicine
IntroductionGorlin–Goltz syndrome is a rare tumor-predisposing condition caused by genetic variants in the PTCH1 and SUFU pathways. The list of genetic variants associated with Gorlin–Goltz syndrome is not yet exhaustive.
Kathrin Oelmeier, Judit Horváth, Rebekka Vogtmann, Matthias Meyer-Wittkopf, Mareike Möllers, Ralf Schmitz, Kathleen Marie Oberste, Daniela Willy   +7 more
doaj   +1 more source

Case Report: Papillary thyroid carcinoma in Goltz-Gorlin syndrome. [PDF]

Front Endocrinol (Lausanne), 2023
Costanza F, Papi G, Corrado S, Pontecorvi A.   +3 more
europepmc   +1 more source

A case of Goldenhar-Gorlin syndrome with unusual association of hypoplastic thumb

Indian Journal of Ophthalmology, 2008
A case of Goldenhar-Gorlin syndrome in a seven-month-old male infant presented with the features of epibulbar dermoid, microtia and hemifacial microsomia associated with thumb defect. The dermoid was bilateral and microtia was unilateral.
Das Amitava, Ray Biswarup, Das Debabrata, Das Somnath   +3 more
doaj  

A case report of Gorlin-Goltz syndrome as a rare hereditary disorder

Journal of Research in Medical Sciences, 2011
Gorlin-Goltz syndrome is an autosomal dominant and a rare hereditary disease. Diagnosis of this syndrome is based on major and minor criteria. We report a Gorlin-Goltz syndrome in a 25-year-old male who was presented with progressive pain of maxilla and ...
Mehri Sirous, Nazila Tayari
doaj  

Gorlin syndrome - Case report. [PDF]

J Dent Sci, 2022
Yeh TH, Chen YC, Lee YP, Chiang CP.
europepmc   +1 more source

Surveillance of a large cardiac fibroma in a patient with Gorlin syndrome. [PDF]

BMJ Case Rep, 2023
Hampal R, Knott K, Marciniak A.
europepmc   +1 more source

Sustained Suppression of Gorlin Syndrome-Associated Basal Cell Carcinomas with Vismodegib or Sonidegib: A Case Series. [PDF]

Curr Oncol, 2023
Wescott R, Samlowski W.
europepmc   +1 more source

An Easily Missed But Life-Threatening Diagnosis: A Case Report of Gorlin Syndrome. [PDF]

Am J Case Rep, 2023
Kosmidis CS, Michael C, Mystakidou CM, Theodorou V, Papadopoulou E, Papadopoulou K, Koulouris C, Varsamis N, Koimtzis G, Roullia P, Ntager M, Sevva C, Katsios NI, Charalampous I, Zarampouka K, Baka S.   +15 more
europepmc   +1 more source