Results 61 to 70 of about 1,227,254 (171)

Multiple Odontogenic Keratocysts as the Initial Manifestation of Gorlin Syndrome in a Child: A Case Report With Conservative Management and Diagnostic Considerations

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Multiple odontogenic keratocysts are one of the major diagnostic criteria of Gorlin syndrome and may represent an early manifestation of the disorder in pediatric patients. This report describes the diagnostic process and management of an 11‐year‐old boy who presented with multiple mandibular cystic lesions associated with displacement of developing ...
V. Anguera-Ortega, P. Cahuana-Bartra, L. Brunet-Llobet, Y. González-Chópite, E. I. Mashala, J. Miranda-Rius, Priya Gusain   +6 more
wiley   +1 more source

Focal dermal hypoplasia: A novel finding in disguise

Journal of Oral Biology and Craniofacial Research, 2018
Focal Dermal Hypoplasia (FDH) or Goltz-Gorlin syndrome is an unusual X-linked dominant syndrome characterised by anomalies of both ectodermal and mesodermal structures.We present a case report on the management of a 58 year old Caucasian male with Focal ...
S. Nathwani, K. Martin, R. Bunyan
doaj   +1 more source

Plaque‐type trichoblastoma and its siblings: A (follicular tumour) family history

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Ines Bertlich, Ferdinand Toberer, Tilman Schulz, Dmitry V. Kazakov, Wolfgang Hartschuh   +4 more
wiley   +1 more source

Syndromic Multiple Odontogenic Keratocysts Associated With Impacted Teeth: A Rare Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Introduction Odontogenic keratocysts are developmental odontogenic cysts that may occur as solitary lesions or as multiple jaw lesions. Multiple odontogenic keratocysts in young patients should raise suspicion of an underlying syndrome, particularly Gorlin–Goltz syndrome.
Faizal Manrapi, Mohammad Gazali, Nurwahida, Nisrina Ekayani Nasrun, Hannah Wesley   +4 more
wiley   +1 more source

Vulvar Apocrine Hidrocystoma: A Rare Case Report

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Apocrine hidrocystoma is a rare and benign tumor that usually occurs on the head, neck, and face. Involvement of the vulva is extremely rare, with only a few documented case reports in the literature. The prognosis of the tumor is favorable with surgical excision, with no reported recurrences.
Nastaran Mahmoudnejad, Peyman Mohammadi Torbati, Niloofar Irandoost, Karuna Sharma   +3 more
wiley   +1 more source

Nevoid basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Case report [PDF]

, 2013
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome (NBCCS) comprises multiple basal cell carcinomas, keratocysts of the jaw, palmar/plantar pits, spine and rib anomalies, calcifications of the falx cerebri etc.
Belli, E., Fini, Giuseppina, Virciglio, Pasquale, Mici, Elidon, D'Itri, L., Pasta, Vittorio, Malavenda, M.S., Krizzuk, D., Maturo, A., Merola, R., Moricca, Luca Maria, Leonardi, A.   +11 more
core   +2 more sources

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 9, September 2025.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio, J. Zhao, S. E. Boyden, R. Mao, P. Bayrak‐Toydemir, A. Pflaum, J. Palumbos, A. Andrews, E. E. Baldwin, C. Welt, Mackenzie Fait, Undiagnosed Diseases Network, L. D. Botto, D. Viskochil   +13 more
wiley   +1 more source

Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology

Developmental Dynamics, Volume 254, Issue 2, Page 102-141, February 2025.
Abstract The ventral body wall (VBW) that encloses the thoracic and abdominal cavities arises by extensive cell movements and morphogenetic changes during embryonic development. These morphogenetic processes include embryonic folding generating the primary body wall; the initial ventral cover of the embryo, followed by directed mesodermal cell ...
Caroline Formstone, Bashar Aldeiri, Mark Davenport, Philippa Francis‐West   +3 more
wiley   +1 more source

Youngest Encounter with Gorlin–Goltz Syndrome: Navigating Early Diagnosis and Management

Indian Journal of Paediatric Dermatology
Gorlin–Goltz syndrome is a rare autosomal dominant disorder caused by an inactivating mutation of the patched 1 gene. Patients could present as early as infancy with varied presentation and multiple basal cell carcinoma.
Adarsh Vijayakumar, Rashmi Mary Philip, Sebastian Criton   +2 more
doaj   +1 more source

The role of electrochemotherapy in the treatment of locally advanced or recurrent eyelid‐periocular basal cell carcinoma: long‐term results

International Journal of Dermatology, Volume 64, Issue 1, Page 111-118, January 2025.
Abstract Background While electrochemotherapy (ECT) is increasingly utilized as a highly effective method in the treatment of tumors in the head and neck region, there is significantly less data available for eyelid‐periocular skin tumors. Our group reported the first extensive case series of eyelid‐periocular basal cell carcinoma (BCC) patients with ...
Attila Vass, Nóra Polgár, Szilvia Alexa Sándor, Dóra Ágoston, Petra Rózsa, Ildikó Csányi, Henriette Ócsai, Eszter Baltás, Judit Oláh, Erika Gabriella Kis, Edit Tóth‐Molnár   +10 more
wiley   +1 more source