Zobrazeno 1 - 10
of 689
pro vyhledávání: '"gorlin-goltz syndrome"'
Autor:
Joanna Mietlińska-Sauter, Elena Varotto, Elżbieta Żądzińska, Wiesław Lorkiewicz, Francesco Maria Galassi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract The anomaly known as a bifid rib is difficult to quantify in bioarchaeological collections not only because of its rarity in the population itself (less than 1.5%), but also because of vulnerability to postmortem damage of this part of the s
Externí odkaz:
https://doaj.org/article/6286898f7cd646ca803d32f169a99e8a
Publikováno v:
BMC Women's Health, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background To demonstrate and analyze the 18F-FDG positron emission tomography/computed tomography (PET/CT) findings in this rare nevoid basal cell carcinoma syndrome (NBCCS). Case presentation A 71-year-old woman with the left invasive brea
Externí odkaz:
https://doaj.org/article/f5274bf5c9104098b2e42477773434e3
Publikováno v:
Indian Journal of Dental Research, Vol 34, Iss 4, Pp 451-454 (2024)
Introduction: Although numerous syndromic and non-syndromic odontogenic lesions of the jaws have been documented in the literature, there are very few cases of simultaneous benign and malignant jaw lesions. Patient Concerns: We present a case of righ
Externí odkaz:
https://doaj.org/article/f45bf70c7bd1401287d4eea41061c894
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Managing advanced basal cell carcinoma (BCC) in patients with Gorlin-Goltz syndrome presents unique clinical challenges due to the tumor’s aggressive nature and potential for widespread metastasis. This case study details a sequential treatment reg
Externí odkaz:
https://doaj.org/article/11e38f4a73c84371b3474e5690ee54ef
Publikováno v:
Clinical and Biomedical Research, Vol 43, Iss 4 (2024)
Hybrid odontogenic lesions combine characteristics of two or more lesions in a single site, and are considered a rare condition. The occurrence of this lesion in a patient with Gorlin-Goltz syndrome is even less common. Since the condition has variab
Externí odkaz:
https://doaj.org/article/ff6da260729d47989bb0f00ed94b8224
Autor:
Paula I. Wilke, Daniel Biermann, Maria Grafmann, Rainer Kozlik-Feldmann, Dzhoy Papingi, Jörg S. Sachweh, Fridrike Stute, Jakob Olfe
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Primary cardiac tumors in children are very rare and may be associated with severe arrhythmias and sudden infant death syndrome. These cardiac arrhythmias vary depending on the location and size of the tumor. Sixty-four percent of children w
Externí odkaz:
https://doaj.org/article/395700dcf33747b0aec49b8d3cb20820
Publikováno v:
Archives of Plastic Surgery, Vol 50, Iss 04, Pp 384-388 (2023)
Gorlin–Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is an autosomal dominant disease characterized by multisystemic developmental defects caused by pathogenic variants such as patched-1 (PTCH1) gene variants and/or SUFU gene
Externí odkaz:
https://doaj.org/article/650f58e358d740609b15c1efa1ca1b75
Autor:
Guilherme Salazar Serrano, Alexandre Dias de Oliveira, Ramsés Miotto, Katia Lin, Guilherme Loureiro Fialho
Publikováno v:
Epilepsy & Behavior Reports, Vol 26, Iss , Pp 100667- (2024)
Epilepsy is one of the most common chronical neurological conditions affecting over 50 million people worldwide. In addition to the stigma and discrimination, individuals with epilepsy suffer from a nearly three-fold increased risk of premature death
Externí odkaz:
https://doaj.org/article/ad76d3a0a7b8448e80bfe9ca1f60821b
Publikováno v:
Contemporary Clinical Dentistry, Vol 14, Iss 4, Pp 317-321 (2023)
Keratocyst is a developmental odontogenic cyst arising from remnants/rests of the dental lamina with biologic behavior similar to benign neoplasm. The presence of multiple odontogenic keratocysts is rare and seen in Gorlin-Goltz syndrome (GGS). GGS s
Externí odkaz:
https://doaj.org/article/84023d8a458140069dda6dd62f28ef92
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