Zobrazeno 1 - 10
of 404
pro vyhledávání: '"Phacomatosis"'
Autor:
Vishalakshi S Pandit, Y R Rakesh
Publikováno v:
Clinical Dermatology Review, Vol 8, Iss 3, Pp 253-255 (2024)
Phacomatosis pigmentovascularis (PPV) is a term used to describe the association of vascular nevi with different pigmentary nevi. There are a very few case reports describing the association of two pigmented nevi or pigmented anomalies of nevoid char
Externí odkaz:
https://doaj.org/article/bf317aba92dd4d1d9f0c5cf5e21968a3
Autor:
Damian, Simona Irina, Stefanescu, Cristinel, Diac, Mădălina Maria, Schiopu, Cristina-Gabriela
Publikováno v:
Buletin de Psihiatrie Integrativa / Bulletin of Integrative Psychiatry. 97(2):63-78
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=1127275
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:
Эпилепсия и пароксизмальные состояния, Vol 12, Iss 1, Pp 67-73 (2020)
The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis and tuberous sclerosis. This disease is not inherited, but occurs exclusively sporadically, both in men and in women, and in all races and ethnic groups. I
Externí odkaz:
https://doaj.org/article/34a476959731402283e7ce8173666e60
Publikováno v:
Medičnì Perspektivi, Vol 24, Iss 4, Pp 182-190 (2019)
In the practical activities of a modern doctor, significant difficulties are noted in the diagnostics and proper management of patients with hereditary diseases due to the limited coverage of the population by genetic researches. For a long time, the
Externí odkaz:
https://doaj.org/article/9eec88c7b7bc44ee98781e9bd973c439
Autor:
Kinan Hayani, Kathrin Giehl, Jörg Kumbrink, Judith Fischer, Max Schlaak, Lars E. French, Andreas Wollenberg
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 15, p adv00241 (2020)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/1df769d34a4b40e585c90a83a404c4ea
Publikováno v:
Русский журнал детской неврологии, Vol 12, Iss 4, Pp 50-55 (2018)
Linear nevus sebaceous is a rare sporadic neuro-oculocutaneous syndrome characterizes by a triad of symptoms: linear nevus sebaceous, lesion of the central nervous system and lesion of the organs of vision. The authors present a brief overview of Rus
Externí odkaz:
https://doaj.org/article/dc727416960a423384aba1fbbb45e7c7
Autor:
Andrea Maria Plateroti, Rocco Plateroti, Roberto Mollo, Aloisa Librando, Maria Teresa Contestabile, Vito Fenicia
Publikováno v:
Case Reports in Ophthalmology, Vol 8, Iss 2, Pp 375-384 (2017)
We present the case of a 12-year-old boy with Sturge-Weber syndrome and ocular melanocytosis who presented with bilateral naevus flammeus of the face and hyperpigmentation of the right iris associated with ipsilateral iris mammillations. The patient
Externí odkaz:
https://doaj.org/article/84d7b4834c71465da3df4df3f7a8301a
Publikováno v:
Kerala Journal of Ophthalmology, Vol 29, Iss 3, Pp 226-229 (2017)
Sturge–Weber syndrome (SWS) is a rare neuro-oculocutaneous disorder. The classical signs are unilateral facial port wine stain, leptomeningeal angiomas, and their sequele with ipsilateral glaucoma. Here, we are reporting two cases of SWS associated
Externí odkaz:
https://doaj.org/article/b872e5213747408cb6875f0fe01143dc