Bart Syndrome Associated with Pyloric Atresia: An Uncommon Case Report

  • سال انتشار: 1402
  • محل انتشار: مجله بین المللی کودکان، دوره: 11، شماره: 5
  • کد COI اختصاصی: JR_INJPM-11-5_015
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 264
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نویسندگان

Homa Babaei

Professor of Neonatal-Perinatal Medicine , Department of Pediatrics, School of Medicine, Imam Reza Hospital , Kermanshah University of Medical Sciences, Kermanshah, Iran

Pourang Mohammadi

Doctor of Medicine, School of Medicine , Kermanshah University of Medical Sciences, Kermanshah, Iran

khadijeh Ramezani-Ali Akbari

Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Soudabeh Ramezani-Ali Akbari

Doctor of Medicine, School of Medicine , Kermanshah University of Medical Sciences, Kermanshah, Iran

Zohre Fatemi

pediatric &congenital cardiology Division,Pediatric Department,Factulty of Medicine , Mashhad University of Medical Sciences, Mashhad,Iran

چکیده

Background: Aplasia cutis congenital type VI (Bart’s syndrome) has been known as an extremely rare genetic disorder in which there is localized absence of skin, epidermolysis bullosa and nail deformities. Case report: Here, we present a rare case of Bart’s syndrome in a female newborn diagnosed with congenital loss of skin over upper and lower limbs, trunk, neck and face as well as some bullae on them. Moreover, a dilated stomach was observed in radiographic examination. We treated the baby with TPN, systemic antibiotics, and also her wounds were covered by topical ointments. Laboratory tests, along with liver and renal function analyses were normal, and also serologic tests for infection were negative but she died at the age of ۴ days. Conclusion: The association between Bart’s syndrome and pyloric atresia is a highly fatal combination and there is no treatment option to rescue the patients.

کلیدواژه ها

Bart' s syndrome,,, ,،absence of skin,,, ,،epidermolysis bullosa,,, ,،pyloric atresia

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