A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition

Deepak Sharma

Article Details

A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition

Authors:

Deepak Sharma

Publisher:

Islamic World Academy of Sciences (IAS)

Journal:

Medical Journal of Islamic World Academy of Sciences Vol.24 Issue 3, pp.96-98

Document Type:

Article

Publication Date:

1/2016

Document Language:

English

Document ID (Org No.):

2001937942

pISSN:

2415-1300

Keywords:

Abstract:

 This study aimed to describe a case of aplasia cutis congenita with epidermolysis bullosa, as only a few reports of Bart’s syndrome exist in the medical literature. Aplasia cutis congenita (ACC) is a rare dermatological condition characterized by the absence of skin. It has no proven etiology and hence stills remains a mystery for the dermatologist of the modern world. The most common body part affected is the scalp. ACC with epidermolysis bullosa (Bart’s syndrome) is a very rare variant of aplasia cutis.

Article Details

A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition

Authors:

Deepak Sharma

Publisher:

Islamic World Academy of Sciences (IAS)

Journal:

Medical Journal of Islamic World Academy of Sciences Vol.24 Issue 3, pp.96-98

Document Type:

Article

Publication Date:

1/2016

Document Language:

English

Document ID (Org No.):

2001937942

pISSN:

2415-1300

Aplasia cutis congenita

Bart’s syndrome

epidermolysis bullosa

neonate

type VII collagen (COL7A1)

Issues

Article Details

A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition

Authors: Deepak Sharma

Publisher: Islamic World Academy of Sciences (IAS)

Journal: Medical Journal of Islamic World Academy of Sciences Vol.24 Issue 3, pp.96-98

Document Type: Article

Publication Date: 1/2016

Document Language: English

Document ID (Org No.): 2001937942

pISSN: 2415-1300

Aplasia cutis congenita

Bart’s syndrome

epidermolysis bullosa

neonate

type VII collagen (COL7A1)

Issues

Authors:

Deepak Sharma

Publisher:

Islamic World Academy of Sciences (IAS)

Journal:

Medical Journal of Islamic World Academy of Sciences Vol.24 Issue 3, pp.96-98

Document Type:

Article

Publication Date:

1/2016

Document Language:

English

Document ID (Org No.):

2001937942

pISSN:

2415-1300