ISSN 2415-1297 (Online)   ISSN 2415-1300 (Print)
 
             
 
Volume : 25 Issue : 2 Year : 2017
 
A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition [Med J Islamic World Acad Sci]
Med J Islamic World Acad Sci. 2016; 24(3): 96-98 | DOI: 10.5505/ias.2016.81905  

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

Deepak Sharma1, Sachin Lamba2, Anshul Maheshwari2, Sweta Shastri3
1Pt B.d. Sharma, Pgims, Rohtak, Haryana, India.
2S.m.s Medical College, Jaipur, Rajasthan, India.
3Nkp Salve Medical College, Nagpur, Maharashtra, India.

This study aimed to describe a case of aplasia cutis congenita with epidermolysis bullosa, as only a few reports of Bartís 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 (Bartís syndrome) is a very rare variant of aplasia cutis.

Keywords: Aplasia cutis congenita, Bartís syndrome, epidermolysis bullosa, neonate, type VII collagen (COL7A1)


Deepak Sharma, Sachin Lamba, Anshul Maheshwari, Sweta Shastri. A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition. Med J Islamic World Acad Sci. 2016; 24(3): 96-98

Corresponding Author: Deepak Sharma, India


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