Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Fatima, Razvi"'
Publikováno v:
Indian Dermatology Online Journal, Vol 15, Iss 2, Pp 270-273 (2024)
Nocardiosis is a rare infection due to a ubiquitous, gram-positive, weakly acid-fast, filamentous, aerobic bacteria, that are usually responsible for opportunistic infection in immunocompromised patients. Less frequently, nocardiosis can affect immun
Externí odkaz:
https://doaj.org/article/fca4fdc76d544bff83585e3bbf1167a2
Autor:
Neha Chowdary Koganti, Nayeem Sadath Haneef, Fatima Razvi, B. Y. Praveen Kumar, Nikhat Fatima, Mohammed Altamash Zubair, Debasmita Chakraborty
Publikováno v:
Journal of Medical and Allied Sciences, Vol 7, Iss 2, Pp 118-121 (2017)
Kindler's syndrome is a rare autosomal recessive disorder. It is characterized by trauma-induced blistering, photosensitivity, poikiloderma and mucosal inflammation. It occurs due to mutation on chromosome 20p. This report describes two siblings wit
Externí odkaz:
https://doaj.org/article/0eac35844c9d44939d2d544c518677fa
Autor:
Mohammed Altamash Zubair, Nayeem Sadath Haneef, Fatima Razvi, B. Y. Praveen Kumar, Nikhat Fatima, Neha Chowdary Koganti
Publikováno v:
Journal of Medical and Allied Sciences, Vol 7, Iss 2, Pp 122-125 (2017)
Dowling Dego's disease is a rare autosomal dominant condition. It is caused by loss of function mutations in keratin 5 gene (kRT5) situated in keratin gene cluster on 12q13. We are reporting three cases of Dowling Dego's disease out of which two belo
Externí odkaz:
https://doaj.org/article/43df726a524d44fca7465ec642261050
Autor:
Debasmita Chakraborty, Nayeem Sadath Haneef, Fatima Razvi, B. Y. Praveen Kumar, Nikhat Fatima, Neha Chowdary Koganti, Mohammed Altamash Zubair
Publikováno v:
Journal of Medical and Allied Sciences, Vol 7, Iss 2, Pp 114-117 (2017)
Psoriasis and vitiligo are autoimmune diseases. Occurrence of both these diseases in the same patient, especially at same sites is uncommon. Here, one such patient having both psoriasis and vitiligo lesions at the same site is being reported. An eigh
Externí odkaz:
https://doaj.org/article/f68c2c49e3d14371908ee6a56f11fc0f
Autor:
Fatima Razvi
Publikováno v:
Journal of Medical and Allied Sciences, Vol 5, Iss 1, Pp 21-23 (2015)
Lupus Erythematosus (LE) is a multi-organ auto-immune disease which results from complex interaction of genetic and environmental factors. The clinical spectrum ranges from minor cutaneous lesions to life threatening multi-organ dysfunction. The skin
Externí odkaz:
https://doaj.org/article/57b96333c5014fbe8c493c0e0501a75a
Autor:
Fatima Razvi, A. S. Kumar
Publikováno v:
Journal of Medical and Allied Sciences, Vol 3, Iss 1, Pp 22-25 (2013)
Primary cutaneous amyloidosis often presents with pigmentary dystonias of the skin in the form of asymptomatic reticulate hyper-pigmentation or pruritic lichenoid papular lesions. The aim of this study was to evaluate the incidence of primary cutaneo
Externí odkaz:
https://doaj.org/article/2ba0bfe45ccf4b9083ae2b57d80a4804
Autor:
Nayeem Sadath Haneef, Sriteja, Ramesh Bang, Fatima Ummul Hasnath, Fatima Razvi, Chudi Kavya Reddy
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 7:1620-1624
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 6:6891-6894
Autor:
Nayeem Sadath Haneef, Debasmita Chakraborty, Fatima Razvi, Neha Koganti, Nikhat Fatima, Mohammed Zubair, Bomma Yadagiri Praveen Kumar
Publikováno v:
Journal of Medical and Allied Sciences, Vol 7, Iss 2, Pp 114-117 (2017)
Psoriasis and vitiligo are autoimmune diseases. Occurrence of both these diseases in the same patient, especially at same sites is uncommon. Here, one such patient having both psoriasis and vitiligo lesions at the same site is being reported. An eigh
Autor:
Bomma Yadagiri Praveen Kumar, Mohammed Zubair, Nikhat Fatima, Neha Koganti, Nayeem Sadath Haneef, Debasmita Chakraborty, Fatima Razvi
Publikováno v:
Journal of Medical and Allied Sciences, Vol 7, Iss 2, Pp 118-121 (2017)
Kindler's syndrome is a rare autosomal recessive disorder. It is characterized by trauma-induced blistering, photosensitivity, poikiloderma and mucosal inflammation. It occurs due to mutation on chromosome 20p. This report describes two siblings wit