نتایج جستجو برای: clinical characteristic
تعداد نتایج: 1316807 فیلتر نتایج به سال:
Atopic dermatitis (AD) is a pruritic, relapsing, chronic disease that arises most commonly during infancy, childhood, or adolescence. It is clear that genetic factors are important in AD, a family history of AD, allergic rhinitis, and/or asthma and other “Atopic” phenomena being common in patient with AD. The two main pathogenetic characteristic of AD are: I) IgE-mediated antigen dependent “Spe...
Introduction: Extranodal Natural Killer (NK)/T-cell lymphoma (NKTCL) nasal type is a rare but well-known disease with poor prognosis. NKTCL is more prevalent in Asia and comprises about 7-10% of all non-Hodgkin lymphoma cases in this region. The characteristic clinical pattern of NKTCL is the destruction of the midline structures of the mid-face. Case Report: The present study examines a case o...
Case Description: A ten-year-old neutered female terrier dog was referred to the Tehran-Azma Veterinary Diagnostic Center for history of too late recovery too late after ovariohysterectomy. Clinical Finding: Blood chemical laboratory tests revealed high serum BUN, maximum concentration of creatinine and decreased of serum albumin. Sonographically, there was an anechoic cyst-like structurein th...
Hutchinson - Gilford syndrome or progeria is a rare genetic disease with failure to thrive, deficiency of pubertal development and dwarfism. These patients die of premature cardiovascular disturbances and other complications. Characteristic clinical features are finely thin skin, small chin, defect in skin adnexals, prominance scalp tends to be further enhanced by frontal and perietet bossing a...
introduction: diabetes mellitus is an growing national and international public health concern. the number of people affected by diabetes in world by 2030 will be 69% in developing countries. regular physical activity plays a key role in the management of type 2 diabetes melitus, particularly glycemic control. it has been recommended that peoples with type 2 diabetes participate in moderate-int...
In December 2019, a new virus called coronavirus disease 2019 (COVID-19) causing severe acute respiratory syndrome emerged in Wuhan, China, and rapidly spread to other areas of China and other regions of the world. Since it was discovery, COVID-19 has spread to several countries and to this date, affecting about 2,329,651 people and caused about 160,721 deaths. Since most COVID-19 infected cas...
objectives: myotonic dystrophy type i (dm1) is a dominantly inherited disorder with a multisystemic pattern affecting skeletal muscle, heart, eye, endocrine and central nervous system. dm1 is associated with the expansion and instability of ctg repeat in the 3' untranslated region of the myotonic dystrophy protein kinase (dmpk) gene located on chromosome 19q13.3. the aim of this study was ...
background : wilson disease (wd) is an autosomal recessive progressive degeneration of hepatolenticular tissue that causes the increase of copper deposition in the liver and other organs, with resultant hepatic, neurologic and psychological manifestations. wd is fatal if left untreated. the aim of the current study was to evaluate the clinical and para-clinical findings in children with wd in s...
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