نتایج جستجو برای: loose skin

تعداد نتایج: 205412  

Journal: :iranian journal of parasitology 0
hossein mortazavi dept. of dermatology, razi hospital, tehran university of medical sciences, tehran, iran. mehdi mohebali dept. of medical parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran and center for research of endemic parasites of iran (crepi), tehran university of medical sciences, tehran, iran. yasaman taslimi molecular immunology and vaccine research laboratory, pasteur institute of iran, tehran, iran. pardis sadeghipour molecular immunology and vaccine research laboratory, pasteur institute of iran, tehran, iran. mahsa ansari dept. of dermatology, razi hospital, tehran university of medical sciences, tehran, iran. kambiz kamyab department of pathology, razi hospital, tehran university of medical sciences, tehran, iran.

herein, a 28-year-old man with hoarseness, skin and oral lesions is presented. at the time of admission, the patient had an erythematous plaque on his chin near his lower lip and an erythematous-violaceous plaque on his palate near the open-ing of the pharynx and 20 kg weight lost in last one year. the biopsy of his skin lesions by hematoxylin and eosin staining revealed an infiltration of the ...

Journal: :Current Biology 1995

Journal: :The American Journal of Sports Medicine 2012

Journal: :Canadian Journal of Disability Studies 2016

Journal: :American Journal of Orthodontics and Dentofacial Orthopedics 2016

Journal: :European Journal of Information Systems 2010

Journal: :Current Biology 1995

2013
Mehdi Alehossein Masoud Pourgholami Kamyar Kamrani Mohammad Soltani Afshin Yazdi Payman Salamati

Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. Three types of congenital cutis laxa have been recognized. Other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. We describe a female neonate involved by cutis laxa syndrome and a positive family history. We focus on the radiologic findings o...

2017
Rakesh Kumar Sheetal Sharda Vimlesh Soni Kaniyappan Nambiyar

Autosomal recessive cutis laxa type-II (ARCLII) is a spectrum of clinical disorders with prenatal and postnatal growth retardation, cutis laxa, dysmorphism, and skeletal abnormalities. We report the case of a 14-month-old boy with developmental delay, hypotonia, dysmorphism, and loose skin. A novel homozygous variant was observed in ATP6VOA2 gene. Clinical spectrum of ARCLII is highly heterogen...

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