Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Snehal Balvant Lunge"'
Publikováno v:
Clinical Dermatology Review, Vol 5, Iss 2, Pp 223-225 (2021)
Porokeratosis (PK) is a rare group of heterogeneous disorders of keratinization representing diverse phenotypic expressions of the same genetic defect, which is mainly inherited in an autosomal dominant manner. This report describes the case of a 40-
Externí odkaz:
https://doaj.org/article/02bbb2571cf84f8696c0b5bffca69959
Autor:
Puneet Agarwal, Snehal Balvant Lunge, Nandini Sundar Shetty, Priyanka Karagaiah, Steven Daveluy, Alex G. Ortega-Loayza, Thrasyvoulos Tzellos, Jacek C. Szepietowski, Christos C. Zouboulis, Stephan Grabbe, Mohamad Goldust
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 13, p 3813 (2022)
Hidradenitis suppurativa/acne inversa (HS) is a chronic inflammatory disease of the pilosebaceous unit leading to formation of painful, inflammatory nodules, abscesses and tunnels in apocrine gland-bearing areas of the skin. Pain and drainage are the
Externí odkaz:
https://doaj.org/article/0112efb3f6b04091a26cd4bcd832144d
Publikováno v:
Indian Journal of Dermatology, Vol 63, Iss 2, Pp 176-179 (2018)
Vitamin D-dependent rickets type II is a rare hereditary disorder. It occurs due to mutations in the gene chr. 12q12-q14, which codes for vitamin D receptor. End-organ resistance to 1,25-(OH)2vitamin D3 and alopecia in severe cases are the characteri
Externí odkaz:
https://doaj.org/article/cb363286fc20440787698c1a6df58194
Publikováno v:
Nasza Dermatologia Online, Vol 8, Iss 4, Pp 457-459 (2017)
Unilateral hyperhidrosis is a rare entity with primary and secondary causes. So far in literature, the associations documented with this entity rarely include neurofibromatosis. This association, however has been reported previously and perhaps is a
Externí odkaz:
https://doaj.org/article/f8fdcc7fe8424653acfc20a395227fec
Publikováno v:
Nasza Dermatologia Online, Vol 6, Iss 2, Pp 317-320 (2015)
Cheilitis granulomatosa (CG) is a chronic swelling of the lip due to granulomatous inflammation. It is a rare inflammatory disorder first described by Miescher in 1945. It is a monosymptomatic form or an incomplete variant of Melkersson-Rosenthal syn
Externí odkaz:
https://doaj.org/article/cd15637b85874a9d81d75354ba412ea2
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 7, Pp 1-4 (2015)
Fever with rash is one of the most common causes of referral to a dermatologist. A plethora of conditions need to be considered in the differential diagnosis. They may be broadly classified into infectious causes, drug reactions, and autoimmune disor
Externí odkaz:
https://doaj.org/article/747f77223dbb40ce8f39fc0cfa7966d8
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 4, Pp 248-252 (2015)
Background: About 25-45% of patients of chronic urticaria (CU) have been stated to have histamine releasing autoantibodies in their blood. The term autoimmune urticaria is increasingly being accepted for this subgroup of patients. Review of the liter
Externí odkaz:
https://doaj.org/article/752ea029d3044bfcb00f55ea3551439f
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 3, Pp 189-192 (2015)
Rhinocerebral mucormycosis is the most common form of mucormycosis occurring commonly in patients of diabetic ketoacidosis. Fungi of the order Mucorales belong to six families, among whom Rhizopus is the most common, while Mucor is a rare cause. We r
Externí odkaz:
https://doaj.org/article/d1cb2827aead4b3f9b4f5bec3fd7c8c6
Autor:
Snehal Balvant Lunge, Vijaya Sajjan, Ashok M. Pandit, B.S. Manjunathswamy, Anshul Agrawal, Shivakumar Patil
Publikováno v:
Nasza Dermatologia Online, Vol 5, Iss 2, Pp 148-150 (2014)
Leukocytoclastic vasculitis (LCV) is a small-vessel vasculitis with a reported incidence rate of 30 cases per million persons per year. It usually presents as a palpable purpuric skin rash on legs, though any part of the body can be affected. LCV ras
Externí odkaz:
https://doaj.org/article/c4b43b20e71f49e4b64510e239260a2d
Autor:
Snehal Balvant Lunge, Pradeep Mahajan
Publikováno v:
Dermatology Practical & Conceptual (2014)
Cutis marmorata telangiectatica congenita (CMTC) is a very rarely occurring congenital disorder with persistent cutis marmorata, telangiectasia, and phlebectasia. This disorder may be associated with cutaneous atrophy and ulceration of the involved s
Externí odkaz:
https://doaj.org/article/28932d8a3a58446f864e22ec80a08b30