Zobrazeno 1 - 10
of 500
pro vyhledávání: '"cutis verticis gyrata"'
Autor:
Muskan Kanotra, Rupinder Kaur, Chirag Pasricha, Pratima Kumari, Ravinder Singh, Varinder Singh, Sheikh F. Ahmad
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101133- (2024)
Cutis Verticis Gyrata (CVG) is an uncommon condition, often classified as primary (idiopathic) or secondary to other diseases or syndromes. Its pathogenesis remains poorly understood, and its association with genetic syndromes is particularly rare. N
Externí odkaz:
https://doaj.org/article/d782e10907804db991a499867b8c37bf
Publikováno v:
Indian Journal of Plastic Surgery, Vol 57, Iss 01, Pp 067-070 (2024)
Cutis verticis gyrata (CVG) is a rare skin condition characterized by ridges and furrows resembling the brain. CVG falls under three categories: primary essential, primary nonessential, and secondary. This case report focuses on primary essential CVG
Externí odkaz:
https://doaj.org/article/0536619b68f44f079b311623e41ccf58
Autor:
Michael G. Buontempo, BS, Lina Alhanshali, BA, Jerry Shapiro, MD, Elizabeth J. Klein, MD, Christina S. Oh, BA, Randie H. Kim, MD, Eduardo A. Rodriguez, MD, Kristen Lo Sicco, MD
Publikováno v:
JAAD Case Reports, Vol 38, Iss , Pp 44-47 (2023)
Externí odkaz:
https://doaj.org/article/b866fbc163144f5e9e0e9924316043eb
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 25, Iss 1, Pp 40-42 (2024)
Cerebriform intradermal nevus (CIN) is one of the causes for secondary cutis verticis gyrata (CVG). Here, we report a 9-year-old boy with well-demarcated swelling over the left temporal area of his scalp since birth. The swelling was about 15 cm × 1
Externí odkaz:
https://doaj.org/article/1b082557c5344e81a8a290058d0a39dc
Publikováno v:
Кубанский научный медицинский вестник, Vol 30, Iss 6, Pp 89-101 (2023)
Introduction. A differential diagnostic search is a crucial method for making a final clinical diagnosis. Lack of clinical thinking leads to tactical errors, both in making a diagnosis and in choosing a therapy algorithm. The problem of iatrogeneses
Externí odkaz:
https://doaj.org/article/ddecd8dc12aa4f7989038b607ad194f7
Autor:
Mohd Altaf Mir, Jaya Jain, Prince Kumar, Rajesh Maurya, Manjit Kaur Rana, Aakansha Giri Goswami
Publikováno v:
Indian Journal of Plastic Surgery, Vol 56, Iss 06, Pp 544-547 (2023)
Bulldog scalp syndrome or cutis verticis gyrata (CVG) is a rare cutaneous disorder with an incidence of just 0.026 to 1 per 100,000 population and cosmetic problems should not be ignored as they can affect the quality of life of patients in social an
Externí odkaz:
https://doaj.org/article/04812ac301df4401994915a99db83208
Autor:
Santiago Díaz-Bejarano, Daniel Ramos-Hernández, Ana-María Camargo-López, Viviana Gómez-Ortega
Publikováno v:
JPRAS Open, Vol 37, Iss , Pp 82-86 (2023)
Background: Cutis verticis gyrata (CVG) is a condition of excessive skin growth and excessive laxity of the scalp, leading to deep furrows and folds that resemble the gyri and outer surface of the brain. Approaches for the treatment of CVG range from
Externí odkaz:
https://doaj.org/article/f5de2196be864252876ef29ea5692985
Akademický článek
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Publikováno v:
Revista Finlay, Vol 12, Iss 3, Pp 352-356 (2022)
Cutis verticis gyrata is a rare pathology of the scalp characterized by the proliferation of subcutaneous cellular tissue and hypertrophy that produces folds and furrows that give it a cerebriform appearance. Although its etiology is still unknown, t
Externí odkaz:
https://doaj.org/article/60bdda1031364f3cac4aea23554290b5
Autor:
Francesca Mercadante, Ettore Piro, Martina Busè, Emanuela Salzano, Arturo Ferrara, Gregorio Serra, Cristina Passarello, Giovanni Corsello, Maria Piccione
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-7 (2022)
Abstract Background Noonan and Noonan-like syndromes are multisystem genetic disorders, mainly with autosomal dominant trasmission, caused by mutations in several genes. Missense pathogenetic variants of SOS1 gene are the second most common cause of
Externí odkaz:
https://doaj.org/article/1123334782094f0f92fb59aba56dd920