نتایج جستجو برای: cutaneous atrophy

تعداد نتایج: 90483  

2013
Kemal OZYURT Halit BAYKAN Perihan OZTURK Emin SILAY

Melanonychia commonly appears as a longitudinal band, starting from the matrix and extending to the tip of the nail plate. Less often it presents a transverse band or may inolve whole nail plate. Cutaneous side effects of hydroxyurea are described in 13% of patients including increased pigmentation, hyperkeratosis, skin atrophy, xerosis, lichenoid eruptions, palmar and plantar keratoderma, cuta...

2015
Gleb Baida Pankaj Bhalla Kirill Kirsanov Ekaterina Lesovaya Marianna Yakubovskaya Kit Yuen Shuchi Guo Robert M Lavker Ben Readhead Joel T Dudley Irina Budunova

Cutaneous atrophy is the major adverse effect of topical glucocorticoids; however, its molecular mechanisms are poorly understood. Here, we identify stress-inducible mTOR inhibitor REDD1 (regulated in development and DNA damage response 1) as a major molecular target of glucocorticoids, which mediates cutaneous atrophy. In REDD1 knockout (KO) mice, all skin compartments (epidermis, dermis, subc...

Journal: :JAAD case reports 2015
Jeff C Donovan

FFA: Frontal fibrosing alopecia LPP: Lichen planopilaris INTRODUCTION Frontal fibrosing alopecia (FFA) is a form of cicatricial alopecia that predominantly affects perimenopuasal and postmenopausal women. Although the precise cause is unknown, it is currently classified as a primary lymphocytic cicatricial alopecia that is closely related to lichen planopilaris (LPP). FFA not only causes scarri...

2012
Luciana Mendes Lisiane Nogueira Virginia Vilasboas Carolina Talhari Sinésio Talhari Mônica Santos Nilton Lins

Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosens...

Journal: :Revista chilena de pediatria 2014
Piotr Brzezinski Samir Ismail Anca Chiriac

The cutaneous lesion of erythema ab Igne are characterized by a reticulate erythema, hyperpigmentation, fine scaling, epidermal atrophy and telangiectasias, and reticulated erythema. We report a case of erythema ab igne on the hands of a 8-year-old girl, induced by classic homemade radiator.

2016
Rajendra Singh Jain Sunil Kumar Trilochan Srivastava

Parry-Romberg syndrome (PRS) is characterized by progressive degeneration and atrophy of the cutaneous, subcutaneous connective tissues, muscles and bones. Classically, PRS is restricted to unilateral face but in 20% of patients may extend to other parts of the body including ipsilateral or contralateral arms, trunk and legs. We report a case of 24-year-old male who presented with insidious ons...

2011
Preethi Balan Subhas Babu Gogineni Shishir Ram Shetty Deepa D'souza

Progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is an uncommon degenerative condition which is poorly defined. It is characterized by a slow and progressive atrophy affecting one side of the face. The onset usually occurs during the first two decades of life. Characteristically, the atrophy progresses slowly for several years, and then it becomes stable. Ophthalmic involve...

Journal: :Avian diseases 2008
J Michael Day Erica Spackman Mary J Pantin-Jackwood

Recently, pathogenesis studies, using genetically distinct turkey-origin reoviruses (TRVs), revealed that poults infected with certain TRV isolates had moderate to severe bursal atrophy, suggesting virus-induced immune dysfunction. In order to characterize the effect of TRV infection on the turkey immune system, classical assays were undertaken to quantify the humoral and cell-mediated immune r...

Journal: :journal of current ophthalmology 0
هرمز شمس hormoz chams حسن بهبودی hassan behboudi فریبا قاسمی fariba ghassemi فریدون دواچی fereydoun davatchi فرهاد شهرام farhad shahram شیدا شمس دواچی sheyda chams-davatchi

purpose : to investigate and compare the causes of blindness in ocular behçet’s disease (bd) in men and women methods : in a retrospective, descriptive investigation from 1976 to 2008, 6,021 bd cases were registered in our bd unit of shariati hospital of tehran university of medical sciences (tums). at the last visit, 187 patients (124 men and 63 women) were blind (vision=1/10 or less) at least...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید