نتایج جستجو برای: congenital esophageal stenosis

تعداد نتایج: 225036  

Journal: :Global Journal of Medical and Clinical Case Reports 2020

Journal: :galen medical journal 0
elham behrangi dermatology department, rasoul akram hospital, iran university of medical sciences, tehran, iran laya yousefian otolaryngology department, rasoul akram hospital, iran university of medical sciences, tehran, iran aliakbar moodi otolaryngologist, ziaiyan hospital, tehran university of medical sciences, tehran, iran zahra azizian dermatology department, rasoul akram hospital, iran university of medical sciences, tehran, iran

background: subglottic stenosis is defined as inflammatory narrowing of the airway. it can be related to trauma, intubation, autoimmune disorders, vascular malformations, infection and congenital abnormalities. pot-wine stain (pws) is a small dermis venous malformation which is present at birth. pws is found on face and neck, but can occur in throat and can cause subglottic stenosis. case repor...

2006
David D. Yuh

● Epidemiology ● Esophageal atresia occurs in about 2.4 of every 10,000 live births, with a slight preponderance in males and children of older or diabetic mothers. Esophageal duplication cysts account for 10 to 15 percent of all foregut duplication cysts and only 5 to 10 percent of all mediastinal cysts. Congenital esophageal stenosis occurs in between 1:25,000 and 1:50,000 live births. Bochda...

Journal: :acta medica iranica 0
mr. mir

a 12 year old child with liodgkin's disease and having received 12 courses of chemotherapy, was referred to thin center with esophageal obstruction. after having performed the necessary investigations, a decision was made to undertake surgery. after surgery, the patient recovered completely and presently enjoys a heallhv life.

Journal: :Clinical genetics 2009
S B Freeman C P Torfs P A Romitti M H Royle C Druschel C A Hobbs S L Sherman

We report Down syndrome (DS)-associated congenital gastrointestinal (GI) defects identified during a 15 year, population-based study of the etiology and phenotypic consequences of trisomy 21. Between 1989 and 2004, six sites collected DNA, clinical and epidemiological information on live-born infants with standard trisomy 21 and their parents. We used chi-squared test and logistic regression to...

Journal: :General Thoracic and Cardiovascular Surgery 2010

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