Results 41 to 50 of about 1,573 (165)
Nevoid basal cell carcinoma syndrome: A case report
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in patch (PTCH), a tumor suppressor gene that has been mapped to ...
Venkatesh K Dodda +3 more
doaj +1 more source
Gingival enlargement following levetiracetam treatment: A clinical case analysis
Abstract This report describes a 21‐year‐old female with a history of epilepsy, diagnosed at age 17, who developed gingival enlargement after being treated with levetiracetam. Her dosage was titrated to 750 mg twice daily, achieving satisfactory seizure control.
Awadh M. Alahmari, Ali M. Alkhathaami
wiley +1 more source
Epidermal Nevi and Epidermal Naevus Syndromes
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini +2 more
wiley +1 more source
Two male patients with nevoid basal cell carcinoma syndrome from Turkey
Nevoid basal cell carcinoma syndrome, also known as Gorlin's syndrome, is a familial autosomal dominant syndrome characterized by multiple basal cell carcinomas, multiple odontogenic keratocysts of the jaws, and skeletal anomalies. Both tumors and
C Tümer, N Er, S Balci, A Ataç
doaj
Background Ovarian sex cord‐stromal tumors (OSCTs) are rare ovarian tumors that can develop from sex cord, stromal cells, or both. OSCTs can be benign or malignant.
Tomoyasu Higashimoto +7 more
doaj +1 more source
Cancer therapy resistance from a spatial‐omics perspective
Spatial omics technologies reveal unprecedented insights into cancer therapy resistance (CTR) by resolving spatial heterogeneity of tumour and microenvironment. This review highlights cutting‐edge spatial omics and computational technologies, showcasing their transformative potential in deciphering CTR mechanisms and uncovering novel diagnostic and ...
Yinghao Zhang +6 more
wiley +1 more source
Here we report the features of 24 BAP1‐inactivated melanocytic tumours including 19 BAP1‐inactivated melanocytomas (BIMs) and five BAP1‐inactivated melanomas. BIMs have a favourable prognosis, even those with multiple copy number aberrations (CNAs).
Joseph S. Durgin +9 more
wiley +1 more source
Nevoid basal cell carcinoma syndrome: A case report
A case of nevoid basal cell carcinoma syndrome is reported. A 47-year-old woman presented with a 10-year history of widespread asymptomatic nodules. Dermatological examination showed multiple hyperpigmented nodules and papules on the face, trunk, and ...
ZHONG Huiting +5 more
doaj +1 more source
What's new? This population‐based case‐control study quantifies the risk of childhood brain tumors following exposure to radiation from computed tomography scans in Finland. Leveraging comprehensive nationwide cancer and computed tomography data and addressing key limitations in previous research, including reverse causation and confounding by ...
Jad Abuhamed +4 more
wiley +1 more source
Nevoid basal cell carcinoma syndrome—case report and genetic study
Nevoid basal cell carcinoma syndrome (also named Gorlin-Goltz syndrome) is a rare disease. Commonly seen features include multiple odontogenic keratocysts (OKCs), nevus-like basal cell carcinoma, and bifid ribs.
Yu-Feng Huang +2 more
doaj +1 more source

