Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Vijayeeta Jairath"'
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 1, Pp 27-30 (2015)
Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfami
Externí odkaz:
https://doaj.org/article/b0b0eba6b0614bcca41bf3676524df2e
Autor:
Vijayeeta Jairath, Madan Mohan, Nidhi Jindal, Paritosh Gogna, Clarify Syrty, Priyadarshini Mookalamada Monnappa, Sarabjit Kaur, Manu Sehrawat
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 5, Pp 326-329 (2015)
Objective: Pityriasis rosea (PR) is an acute self-limiting disease. Despite vigorous efforts by generations of researchers since nearly 150 years, present treatment modalities for PR are not very gratifying. Ultraviolet radiation has been recommended
Externí odkaz:
https://doaj.org/article/1fb5d1c9f5754fd095f1beb5c973d49e
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 1, Pp 78-80 (2016)
Trichoepithelioma is a rare benign adnexal tumor which may be of solitary nonfamilial type or multiple familial trichoepitheliomas. Here, we describe a rare presentation of nonfamilial case of trichoepithelioma in a 50-year-old female with multiple s
Externí odkaz:
https://doaj.org/article/4c11780f196442c08aa0570242273d77
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 3, Pp 239-241 (2016)
Ichthyosis hystrix (IH) is a rare, genetically, and clinically heterogeneous group of ichthyosiform dermatoses characterized by spiny hyperkeratotic scales. It is inherited either as an autosomal dominant or a sporadic variety. The phenotypic express
Externí odkaz:
https://doaj.org/article/8a956cb5ee204a57b3f0053a8d52de2d
Publikováno v:
Indian Journal of Dermatology, Vol 60, Iss 4, Pp 422-422 (2015)
Cutaneous larva migrans (CLM) is the most common tropically acquired dermatosis caused by infection with hookworm larvae. It is commonly seen in tropical areas, and in people who have a history of foreign travel and of walking barefoot on sandy soil
Externí odkaz:
https://doaj.org/article/6653bbc795d84b85ae5ca30af8d35564
Autor:
Clarify Syrty, Nidhi Jindal, Madan Mohan, Sarabjit Kaur, Paritosh Gogna, Manu Sehrawat, Priyadarshini Mookalamada Monnappa, Vijayeeta Jairath
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 5, Pp 326-329 (2015)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
Objective: Pityriasis rosea (PR) is an acute self-limiting disease. Despite vigorous efforts by generations of researchers since nearly 150 years, present treatment modalities for PR are not very gratifying. Ultraviolet radiation has been recommended
Autor:
Sarabjit Kaur, Surbhi Dayal, Poonam Verma, Nidhi Jindal, Manu Sehrawat, Paritosh Gogna, Vijayeeta Jairath, Vijay Kumar Jain
Publikováno v:
Dermatologic Surgery. 40:1022-1027
Sclerotherapy is a safe, effective, and easily available treatment modality, its role in cherry hemangioma is still unexplored.This study aims at establishing the role and efficacy of sclerotherapy in treating cherry angiomas and its dermatological c
Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 61, Iss 1, Pp 78-80 (2016)
Indian Journal of Dermatology, Vol 61, Iss 1, Pp 78-80 (2016)
Trichoepithelioma is a rare benign adnexal tumor which may be of solitary nonfamilial type or multiple familial trichoepitheliomas. Here, we describe a rare presentation of nonfamilial case of trichoepithelioma in a 50-year-old female with multiple s
Autor:
Parul Aggarwal, Sarabjit Kaur, Surabhi Dayal, Sunny Virdi, Vijay Kumar Jain, Vijayeeta Jairath, Nidhi Jindal
Publikováno v:
Kaur, Sarabjit; Aggarwal, Parul; Jindal, Nidhi; Dayal, Surabhi; Jairath, Vijayeeta; Jain, Vijay Kumar; et al.(2015). Harlequin syndrome: a mask of rare dysautonomic syndromes. Dermatology Online Journal, 21(4). Retrieved from: http://www.escholarship.org/uc/item/3q39d7mz
Harlequin syndrome (HS) is a rare disorder of the sympathetic nervous system which presents with unilateral decreased sweating and flushing of the face, neck, and chest in response to heat, exercise, or emotional factors. The contralateral side displ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e07c14578616633bcb96646158790d8
http://www.escholarship.org/uc/item/3q39d7mz
http://www.escholarship.org/uc/item/3q39d7mz
Autor:
Sarabjit, Kaur, Nidhi, Jindal, Surabhi, Dayal, Vijay Kumar, Jain, Vijayeeta, Jairath, Sunny, Virdi
Publikováno v:
Dermatology online journal. 20(7)
Griscelli Syndrome (GS) is a rare autosomal recessive disorder characterized by pigmentary dilution of the hair and skin (partial albinism). Three different types (1-3) caused by mutation in three different genes have been described. Patients with GS