Type VI Aplasia Cutis Congenita: Bart’s Syndrome

المؤلفون المشاركون

Kulalı, Ferit
Bas, Ahmet Yagmur
Kale, Yusuf
Celik, Istemi Han
Demirel, Nihal
Apaydın, Sema

المصدر

Case Reports in Dermatological Medicine

العدد

المجلد 2015، العدد 2015 (31 ديسمبر/كانون الأول 2015)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2015-11-01

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الأمراض

الملخص 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.

نمط استشهاد جمعية علماء النفس الأمريكية (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

نمط استشهاد الجمعية الأمريكية للغات الحديثة (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

نمط استشهاد الجمعية الطبية الأمريكية (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

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1058369