Zobrazeno 1 - 10
of 245
pro vyhledávání: '"Neurocutaneous Disorder"'
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 2 (2024)
Sturge- Weber syndrome (SWS), is a rare neuro-cutaneous angiomatosis which affects male and females alike. The clinical manifestations include angiomas, haemangiomas of the lips, tongue and palatine region. The oral manifestations are usually unilate
Externí odkaz:
https://doaj.org/article/c2a8bc41737849e3bc98180563c2cd1b
Publikováno v:
Apollo Medicine, Vol 18, Iss 3, Pp 208-211 (2021)
Tuberous sclerosis complex (TSC) is a rare multisystem neurocutaneous disorder associated with the growth of benign tumors in different organs such as the brain, lungs, kidneys, heart, and eyes. The dermatological findings of this disorder are very c
Externí odkaz:
https://doaj.org/article/c9e8420eae6b4cd28e161f9cbf397281
Autor:
Low Qin Jian, Lim Tzyy Huei, Hon Shu Ann, Cheo Seng Wee, Noranizah Binti Wagino, Evelyn Yap Wen Lee
Publikováno v:
Malaysian Family Physician, Vol 16, Iss 3, Pp 101-103 (2021)
Skin conditions are a common reason for consulting primary health care. The public frequently expects their primary health care providers to be able to recognise and treat common skin conditions with confidence. Primary care providers must be able to
Externí odkaz:
https://doaj.org/article/5ad3f9c704c34b39907114cacebc3ff9
Autor:
Evelyn Yap Wen Yee
Publikováno v:
Malaysian Family Physician, Vol 16, Iss 2, Pp 70-72 (2021)
Melkersson-Rosenthal Syndrome (also termed “Miescher-Melkersson-Rosenthal Syndrome”) or (MRS), is a rare neurocutaneous disorder characterized by the clinical triad of recurring facial nerve paralysis, swelling of one or both lips and fissural to
Externí odkaz:
https://doaj.org/article/626e49f56bc849fc95e1092b1c7ea528
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Clévia Rosset, Mariane da Cunha Jaeger, Eduardo Filippi-Chiela, Larissa Brussa Reis, Ivaine Taís Sauthier Sartor, Cristina Brinckmann Oliveira Netto, Caroline Brunetto de Farias, Rafael Roesler, Patricia Ashton-Prolla
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 4 (2021)
Abstract Tuberous sclerosis complex (TSC) is an autosomal dominant cancer predisposition disorder caused by heterozygous mutations in TSC1 or TSC2 genes and characterized by mTORC1 hyperactivation. TSC-associated tumors develop after loss of heterozy
Externí odkaz:
https://doaj.org/article/fe7d672f066a416495abc777371618de
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 19, Iss 1, Pp 68-70 (2018)
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder which is mostly lethal for males. It effects hair, teeth, nails, eyes and central nervous system along with skin. A twelve day old female patient was referred to the dermatology departm
Externí odkaz:
https://doaj.org/article/18bffb62a963434d84e55d2573bfea0a
Publikováno v:
Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 9, Iss 3, Pp 328-330 (2016)
Haberland syndrome, also known as encephalocraniocutaneous lipomatosis, is a rare, congenital neurocutaneous disorder. It is characterized by unilateral central nervous system, cutaneous, and ocular anomalies. We report here a case of 28-year-old fem
Externí odkaz:
https://doaj.org/article/4d9663d5bc03443cb705ccde5b6f0c94