Zobrazeno 1 - 10
of 262
pro vyhledávání: '"Subependymal nodules"'
Autor:
Imad Bougrine, MD, Kenza Berrada, MD, Salma El Houss, MD, Najwa Ech-Cherif Kettani, PhD, Meriem Fikri, PhD, Mohamed Jiddane, PhD, Firdaous Taoursa, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3637-3642 (2024)
Tuberous sclerosis complex is a multisystem genetic disease with autosomal dominant inheritance, characterized by the development of benign tumors known as hamartomas that affect multiple organs. It is a condition with a wide phenotypic spectrum, and
Externí odkaz:
https://doaj.org/article/30768ba90d6442688d08eb95e77a0328
Publikováno v:
Zhongguo linchuang yanjiu, Vol 36, Iss 11, Pp 1708-1712,1717 (2023)
Objective To analyze the clinical,CT and MRI characteristics of tuberous sclerosis complex (TSC) to raise awareness of multiple organ damage in this disease. Methods The clinical, CT and MRI characteristics of 12 cases of clinically confirmed TSC in
Externí odkaz:
https://doaj.org/article/f02f7259ca0a4a9cac35189b589b626e
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundTuberous Sclerosis Complex (TSC) is a hereditary condition that leads to the development of non-malignant neoplasms in various organs, including cardiac rhabdomyomas, which can cause significant complications.Case presentationThis report de
Externí odkaz:
https://doaj.org/article/c1b33ba533d6471395e378f76587b153
Akademický článek
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Autor:
Gokcen Coban, Ekim Gumeler, Safak Parlak, Bahadir Konuskan, Jale Karakaya, Dilek Yalnizoglu, Banu Anlar, Kader K. Oguz
Publikováno v:
Insights into Imaging, Vol 13, Iss 1, Pp 1-9 (2022)
Abstract Objective The generation of numerous sequences and quantitative data in a short scanning time is the most potential advantage of Synthetic MRI (SyMRI). We aimed to test detection of the tubers and to determine underlying tissue characteristi
Externí odkaz:
https://doaj.org/article/1be4c1bf5ec849a983f17c444721d720
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Tuberous sclerosis complex (TSC) is a rare genetic multisystem disorder that was first described by Von Recklinghausen. We describe a case of a female, who initially presented with hematuria and was later found to have multiple manifestation
Externí odkaz:
https://doaj.org/article/8681ab5822c3496ca91181e2b0546b8b
Publikováno v:
Interdisciplinary Neurosurgery, Vol 24, Iss , Pp 101047- (2021)
Introduction: Subependymal giant cell astrocytoma (SEGA) is the most common central nervous system neoplasm in patients with tuberous sclerosis complex (TSC). Pathologic brain lesions include cortical tubers, subependymal nodules (SENs), subependymal
Externí odkaz:
https://doaj.org/article/5316b5e1b91d432e9a1497770aa052a1
Publikováno v:
Journal of Clinical Ophthalmology and Research, Vol 7, Iss 3, Pp 130-134 (2019)
A 22-year-old female with severe headache was referred to eye outpatient department for fundus examination with a possibility of intracranial space-occupying lesion. On fundus examination, we found bilateral disc edema with creamy white elevated lesi
Externí odkaz:
https://doaj.org/article/1025f0b6f1a94a0290ea8d4514048143
Autor:
Nikolas Boy, Jana Heringer, Renate Brackmann, Olaf Bodamer, Angelika Seitz, Stefan Kölker, Inga Harting
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-13 (2017)
Abstract Background Without neonatal initiation of treatment, 80–90% of patients with glutaric aciduria type 1 (GA1) develop striatal injury during the first six years of life resulting in a complex, predominantly dystonic movement disorder. Onset
Externí odkaz:
https://doaj.org/article/ab9c771894e4476fa501ad0826f01b65
Publikováno v:
Contemporary Clinical Dentistry, Vol 7, Iss 2, Pp 236-239 (2016)
Tuberous sclerosis complex is an unusual autosomal dominant neurocutaneous syndrome characterized by the development of benign tumors affecting different body systems affecting the brain, skin, retina, and viscera. It is characterized by cutaneous ch
Externí odkaz:
https://doaj.org/article/7c1186c837064f49a78d5ab14f2500b3