نتایج جستجو برای: congenital esophageal stenosis

تعداد نتایج: 225036  

Journal: :Open Journal of Obstetrics and Gynecology 2023

VACTERL association represents a rare condition with broad spectrum of coexisting congenital abnormalities. Although multifactorial origin has been described, the etiology is still unclear. Prenatal diagnosis can be challenging, as specific characteristics may difficult to determined before birth. This case report describes finding multiple abnormalities in male fetus at 30 weeks gestation. The...

2013
Laurent Michaud Frédéric Coutenier Guillaume Podevin Arnaud Bonnard François Becmeur Naziha Khen-Dunlop Frédéric Auber Aude Maurel Thomas Gelas Martine Dassonville Corinne Borderon Alain Dabadie Dominique Weil Christian Piolat Anne Breton Djamal Djeddi Alain Morali Florence Bastiani Thierry Lamireau Frédéric Gottrand

BACKGROUND Congenital esophageal stenosis (CES) is a rare condition frequently associated with esophageal atresia (EA). There are limited data from small series about the presentation, treatment, and outcomes of CES. METHODS Medical records of all patients with CES included in the French Network on Esophageal Malformations and Congenital Diseases were reviewed retrospectively with regard to d...

Journal: :acta medica iranica 0
p. akbari asbagh a. shahmohammadi

soon after successful results of balloon valvuloplasty in treatment of congenital pulmonary stenosis, use of this technique for relief of congenital aortic stenosis (as) was attempted in different parts of the world. with the purpose of assessment the value of valvuloplasty in comparison with surgical valvotomy in relief of congenital as, we retrospectively studied 115 patients with valvar as, ...

Journal: :Journal of Indian Association of Pediatric Surgeons 2016

Journal: :گوارش 0
nasser ebrahimi daryani mahsa abbaszadeh

kindler syndrome is a rare hereditary disorder that predominantly involves the skin and mucous membrane. acral skin blistering, progressive photosensivity, skin atrophy and poikiloderma that begin from infancy and childhood are considered to be characteristic manifestations. urethral, anal, esophageal, mouth and laryngeal mucosa may be involved in this syndrome, thus periodontitis and gingival ...

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