Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Snežana Minić"'
Autor:
Snežana Minić, Nataša Cerovac, Ivana Novaković, Slobodan Gazikalović, Svetlana Popadić, Dušan Trpinac
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1300 (2023)
Incontinentia pigmenti (IP) is a rare skin disease combined with anomalies of the teeth, eyes, and central nervous system (CNS). Mutations of the IKBKG gene are responsible for IP. Among the most frequent CNS abnormalities found in IP using magnetic
Externí odkaz:
https://doaj.org/article/581be68129d3486197b88ad4ca2d5e9d
Autor:
Snežana Minić, Dušan Trpinac, Ivana Novaković, Nataša Cerovac, Danijela Dobrosavljević Vukojević, Jérémie Rosain
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1711 (2022)
Rare diseases represent a diagnostic challenge due to their number, variety of clinical phenomena, and possibility of a simultaneous presence of two or more diseases. An illustration of this challenge is an occurrence of a late diagnosis of a proband
Externí odkaz:
https://doaj.org/article/995e8b2ab52341f284c9c159dd9bb147
Autor:
Miloš Radičević, Snežana Minić
Publikováno v:
Medicinski podmladak. 73:40-46
Introduction: Bullous pemphigoid is an autoimmune bullous dermatosis that most commonly occurs in elderly patients. Due to its pathogenesis and treatment of the disease, it can also affect the development of comorbidities. Aim: Determination of comor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83f257dc2159081f2c6a7841a2e682df
https://doi.org/10.5937/mp73-33455
https://doi.org/10.5937/mp73-33455
Autor:
Aleksandra Zelenović, Snežana Minić
Publikováno v:
Medicinski podmladak. 69:36-41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3bdabed2f429617bc90ce7b311aacac
https://doi.org/10.5937/mp69-13863
https://doi.org/10.5937/mp69-13863
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 11-12, Pp 752-754 (2015)
Introduction. Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis. Mutations of the IKBKG gene are responsible for IP. A deletion of exons 4-10 can be found in 80% of patients with IP. There are 69 different mutations of the IKBKG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0838f13b792dc4d96d97f1ed3cd22133
http://www.doiserbia.nb.rs/img/doi/0370-8179/2015/0370-81791512752M.pdf
http://www.doiserbia.nb.rs/img/doi/0370-8179/2015/0370-81791512752M.pdf
Publikováno v:
Medical Hypotheses. 81:671-674
In X-chromosome-linked skin disorders the pattern of involvement follows Blaschko lines. Patterns of changes analogous to cutaneous Blaschko lines in different X-linked diseases existed in other organs. There is no commonly accepted analogy to Blasch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4755f054e894c6761ea739e360367788
https://doi.org/10.1016/j.mehy.2013.07.024
https://doi.org/10.1016/j.mehy.2013.07.024
Publikováno v:
Clinical Oral Investigations. 10:343-347
One of interesting aspects in dermatology is the fact that skin may reflect the presence of anomalies in other organs and tissues. One such example is incontinentia pigmenti (IP), a rare, complex, X-linked genodermatosis. Clinical manifestations of I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd2a2b20434125d4392d67c544d32281
https://doi.org/10.1007/s00784-006-0066-z
https://doi.org/10.1007/s00784-006-0066-z
Publikováno v:
Clinical oral investigations. 17(1)
Incontinentia pigmenti (IP) is an X-linked genodermatosis caused by a mutation of the IKBKG gene. The objective of this study was to present a systematic review of the dental and oral types of anomalies, to determine the total number and sex distribu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc983a8043dd161b4c0b3cd3c029a1c4
https://pubmed.ncbi.nlm.nih.gov/22453515
https://pubmed.ncbi.nlm.nih.gov/22453515
Publikováno v:
Dermatology Practical & Conceptual, Vol 12, Iss 3 (2022)
Introduction: Incontinentia pigmenti (IP) is a rare X-linked geno-dermatosis characterized by numerous findings. Skin biopsy and histopathological analysis are considered as minor criteria for the diagnosis of IP. We assume that dermoscopy can assist
Externí odkaz:
https://doaj.org/article/998f94c31b094a858c60461e0be64916
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 8, Iss 1, p 25 (2013)
Orphanet Journal of Rare Diseases, Vol 8, Iss 1, p 25 (2013)
The objective of this study was to present a systematic review of the central nervous system (CNS) types of anomalies and to consider the possibility to include CNS anomalies in Incontinentia pigmenti (IP) criteria. The analyzed literature data from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af84197143656920df56f56c4a128d65