نتایج جستجو برای: diagnosis delay

تعداد نتایج: 587978  

Journal: :Canadian Medical Association Journal 2009

احسانی‌پور, فهیمه,

    Introduction: Cornelia de lange syndrome(CDLS) is a rare syndrome which is characterized by multiple congenital anomalies, mental retardation, characteristic facial appearance, developmental delay, skeletal malformation, hirsutism, and various ophthalmologic problems. The diagnosis of this syndrome is clinical. Case Report: The patient of the present case report was an infant with cornelia ...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
راضیه فلاح r fallah

biotin is a water-soluble vitamin and co-factor for activation of carboxylases apoenzymes. biotinidase enzyme is essential for release of biotin from apoenzymes. absence of biotinidase is an autosomal recessive trait with a prevalence of 1 in 60000. clinical manifestations of biotinidase deficiency include dermatitis, alopecia, seizures, hypotonia, developmental delay, hearing loss, visual impa...

Journal: :The Laryngoscope 2016
Matthew M Smith Anish Abrol Glendon M Gardner

OBJECTIVES/HYPOTHESIS To see if there has been a decrease in patient delay, professional delay, diagnostic delay, and treatment delay in laryngeal cancer. STUDY DESIGN Institutional review board-approved retrospective chart review of patients diagnosed with laryngeal cancer. METHODS Nine hundred sixty-six patients with International Classification of Diseases, Ninth Revision code for laryng...

Journal: :Gastroenterology 2013
Alain M Schoepfer Ekaterina Safroneeva Christian Bussmann Tanja Kuchen Susanne Portmann Hans-Uwe Simon Alex Straumann

BACKGROUND & AIMS Development of strictures is a major concern for patients with eosinophilic esophagitis (EoE). At diagnosis, EoE can present with an inflammatory phenotype (characterized by whitish exudates, furrows, and edema), a stricturing phenotype (characterized by rings and stenosis), or a combination of these. Little is known about progression of stricture formation; we evaluated stric...

ژورنال: توانبخشی 2013

Rubinstein Taybi syndrome is a rare genetic abnormality that includes such features as facial abnormalities, broad thumbs on the hands and feet, small stature, and developmental delay (including fine and gross motor, communication, problem solving, personal-social delays). This case report represents a 12 months old male baby, was referred for his Developmental Delay, and after investigations a...

Journal: :iranian journal of allergy, asthma and immunology 0
bahram mir saeid ghazi asghar aghamohammadi ali kouhi abolhassan farhoudi mostafa moin nima rezaei

primary immunodeficiencies (pid) are a group of disorders, characterized by an unusual susceptibility to infections. delay in diagnosis results in increased morbidity and mortality in affected patients. the purpose of this study was to determine the mortality rate of iranian immunodeficient patients referred to children medical center hospital affiliated to tehran university of medical sciences...

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