Type VI Aplasia Cutis Congenita: Bart’s Syndrome
Joint Authors
Kulalı, Ferit
Bas, Ahmet Yagmur
Kale, Yusuf
Celik, Istemi Han
Demirel, Nihal
Apaydın, Sema
Source
Case Reports in Dermatological Medicine
Issue
Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2015-11-01
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
Bart’s syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa.
We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin.
Bart’s syndrome (BS) is diagnosed clinically based on the disorder’s unique signs and symptoms but histologic evaluation of the skin can help to confirm the final diagnosis.
The patient was managed conservatively with topical antibacterial ointment and wet gauze dressing.
Periodic follow-up examinations showed complete healing.
We emphasized that it is important to use relatively simple methods for optimal healing without the need for complex surgical interventions.
American Psychological Association (APA)
Kulalı, Ferit& Bas, Ahmet Yagmur& Kale, Yusuf& Celik, Istemi Han& Demirel, Nihal& Apaydın, Sema. 2015. Type VI Aplasia Cutis Congenita: Bart’s Syndrome. Case Reports in Dermatological Medicine،Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1058369
Modern Language Association (MLA)
Kulalı, Ferit…[et al.]. Type VI Aplasia Cutis Congenita: Bart’s Syndrome. Case Reports in Dermatological Medicine No. 2015 (2015), pp.1-3.
https://search.emarefa.net/detail/BIM-1058369
American Medical Association (AMA)
Kulalı, Ferit& Bas, Ahmet Yagmur& Kale, Yusuf& Celik, Istemi Han& Demirel, Nihal& Apaydın, Sema. Type VI Aplasia Cutis Congenita: Bart’s Syndrome. Case Reports in Dermatological Medicine. 2015. Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1058369
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1058369