نتایج جستجو برای: behcets syndrome diagnosis

تعداد نتایج: 1029070  

Journal: Surgery and Trauma 2015

Pancoast tumor accounts for 3%-5% of all non-small cell lung carcinomas. This tumor has a distinct clinical presentation through local invasion and the resulting clinical entity called Pancoast syndrome. This syndrome includes severe shoulder pain, arm pain, and Horner’s syndrome andatrophy of forearm and hand muscles. The differential diagnosis of arm and shoulder pain is extensive. Thoracic o...

اسپندار, رامین, ذولفقاری, رویا, سبحانی, امیر, شجیرات, زینب, فرزان, محمود, مازوچی, حامد,

Background: Carpal tunnel syndrome is the most common focal neuropathy that results from pressure on a nerve. The goal of this study was to assess carpal tunnel syndrome and its associated factors such as occupation, sex, and accompanying complications in a teaching general hospital. Methods: This cross-sectional study investigated 362 patients with the diagnosis of carpal tunnel syndrome admi...

Journal: :iranian journal of public health 0
m sahebjamee dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran ng ameri dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran dd farhud genetic clinic, vallie asr sq., 16 keshavarz blvd, tehran, iran.

noonan syndrome is an autosomal dominant disorder that is typically evident at birth. in many affected individuals, this syn­drome is associated with cardiac defects and a distinctive facial appearance. the high frequency of cardiac disorder, oph­thalmic, growth and orthopedic signs, associated with noonan syndrome emphasizes the need for early diagnosis. this re­port aimed to present a 19 year...

Abhimanyu Bhattacharya, Aditya Kanoi, Ashwin Alke Pai, Madhumita Gupta, Raghavendra Sawarappa, Ravi Ramachandra, Subhakanta Mohapatra,

Apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. We present an atypical phenotype of this syndrome with right sided unilateral coronal synostosis. However, type I apert hand and other clinical and radiological features suggestthe diagnosis. Genetic analysis revealed an absence of ...

Journal: :world journal of plastic surgery 0
madhumita gupta department of plastic and reconstructive surgery, ipgme & r, kolkata, india ashwin alke pai department of plastic and reconstructive surgery, ipgme & r, kolkata, india abhimanyu bhattacharya department of plastic and reconstructive surgery, ipgme & r, kolkata, india ravi ramachandra department of plastic and reconstructive surgery, ipgme & r, kolkata, india raghavendra sawarappa department of plastic and reconstructive surgery, ipgme & r, kolkata, india subhakanta mohapatra department of plastic and reconstructive surgery, ipgme & r, kolkata, india

apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. we present an atypical phenotype of this syndrome with right sided unilateral coronal synostosis. however, type i apert hand and other clinical and radiological features suggestthe diagnosis. genetic analysis revealed an absence of ...

امینی, علی,

Ballantyne syndrome is a syndrome with severe hydropic placenta and fetus followed by maternal hydrops. Several different causes may lead to this syndrome. In fact, Ballantyne syndrome may result from any factor causing severe hydrops fetalis. The diagnosis can be supported by sudden and rapid weight gain, severe edema, oliguria with albuminuria, blood pressure less than 140 mmHg and hemo...

Journal: :گوارش 0
ahmad khodadad mehri najafi-sani fatemeh famouri v modaresi

allgrove syndrome also known as triple-a syndrome is an autosomal recessive disorder characterized by alacremia, achalasia and acth-resistant adrenal insufficiency. although this syndrome is rare, herein we report four cases with different clinical manifestations. they were referred to the gastrointestinal ward during a one year period with complaints of vomiting and dysphagia. the diagnosis of...

Background: The treatment of acute promyelocy!c leukemia with all-trans-re!noic acid (ATRA) some!mes results in a syndrome characterized by fever, respiratory distress, weight gain, pleural or pericardial effusion, and pulmonary infiltrates. We report the major clinical and radiologic features of ATRA syndrome. Materials and Methods: In the past, occasional case reports and literature pertainin...

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