Assessment of melanin distribution in epidermolysis bullosa simplex with mottled pigmentation: A case report

2021 ◽  
Author(s):  
Jen‐Ping Chao ◽  
Jing‐Yi Lin ◽  
Cheng‐Ying Chiang ◽  
Tyng‐Shiuan Hsieh ◽  
Sung‐Jan Lin ◽  
...  
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Simplex

Epidermolysis bullosa simplex with mottled pigmentation: a case report

2009 ◽  
Vol 48 (7) ◽  
pp. 753-754 ◽  
Author(s):  
Christian Andres ◽  
Wenchieh Chen ◽  
Heidelore Hofmann ◽  
Johannes Ring ◽  
Christina Schnopp
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Simplex

scholarly journals A Novel Mutation of KRT14 Gene in a Newborn with Epidermolysis Bullosa Simplex (Dowling-Meara Type): Case Report

Perinatology ◽  
2020 ◽  
Vol 31 (1) ◽  
pp. 39
Author(s):  
Sung-min Lim ◽  
Jin hee Kim ◽  
Yeseul Kim ◽  
Seung Sam Paik ◽  
Jeong Eun Kim ◽  
...  
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Novel Mutation ◽  
Epidermolysis Bullosa Simplex

scholarly journals Inherited Epidermolysis Bullosa: A case report

2015 ◽  
Vol 3 (3) ◽  
pp. 39-42 ◽  
Author(s):  
Shyam Kumar Mahato ◽  
Susana Lama ◽  
Nikhil Agarwal ◽  
Nagendra Chaudhary
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Neonatal Period ◽  
Heterogeneous Group ◽  
Mechanical Trauma ◽  
Epidermolysis Bullosa Simplex ◽  
Blister Formation ◽  
Inherited Epidermolysis Bullosa ◽  
Genetically Determined ◽  
Degrees Of Severity

Epidermolysis bullosa (EB) is a heterogeneous group of genetically determined, mechano-bullous disorders characterized by blister formation in response to mechanical trauma. The blistering of the skin occurs in the varying degrees of severity and can severely incapacitate the life of the afflicted patient. Epidermolysis Bullosa Simplex (EBS), the most commonly occurring type, is dominantly inherited where treatment still remains a major challenge. We report a newborn female with blistering of the skin during the immediate neonatal period.

scholarly journals Management of epidermolysis bullosa simplex in pregnancy: A case report

2019 ◽  
Vol 24 ◽  
pp. e00140
Author(s):  
Nidhi Shah ◽  
Sangeeta Kumaraswami ◽  
Juliet E. Mushi
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Simplex ◽  
In Pregnancy

Negative pressure wound treatment in a neonate with epidermolysis bullosa simplex severe generalized: A case report

2020 ◽  
Vol 37 (6) ◽  
pp. 1218-1220
Author(s):  
Anna‐Barbara Schlueer ◽  
Agnes Schwieger‐Briel ◽  
Martin Theiler ◽  
Kathrin Neuhaus ◽  
Clemens Schiestl ◽  
...  
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Negative Pressure ◽  
Wound Treatment ◽  
Epidermolysis Bullosa Simplex

scholarly journals Epidermolysis bullosa simplex: A case report

2012 ◽  
Vol 39 (4) ◽  
Author(s):  
O Peterside ◽  
OE Kunle-Olowu ◽  
OO Adeyemi ◽  
FO Akinbami ◽  
J Omene
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Simplex

Respiratory tract involvement in a child with epidermolysis bullosa simplex with plectin deficiency: A case report

2010 ◽  
Vol 74 (3) ◽  
pp. 302-305 ◽  
Author(s):  
Irena Babić ◽  
Maja Karaman-Ilić ◽  
Nives Pustišek ◽  
Slobodna Sušić ◽  
Ivančica Škarić ◽  
...  
Keyword(s):  
Case Report ◽  
Respiratory Tract ◽  
Epidermolysis Bullosa ◽  
Epidermolysis Bullosa Simplex ◽  
Tract Involvement

scholarly journals Blistering in a newborn: a rare case report

2020 ◽  
Vol 6 (3) ◽  
pp. 432
Author(s):  
Jasleen Kaur ◽  
Jyoti Budhwar ◽  
Ankush Maheshwary ◽  
Karandeep Singh Bhatti
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Skin Biopsy ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Epidermolysis Bullosa Simplex ◽  
Lower Lip ◽  
Minimal Trauma ◽  
Rare Case Report ◽  
Female Baby

<p>Epidermolysis bullosa is a heterogeneous group of inherited mechanobullous disorders that present with skin and mucosal fragility, leading to blister formation after minimal trauma. 18 days old female baby presented with fluid-filled blisters of variable sizes over the lower lip, bilateral heels, hands, buttocks, chest, legs and arms, which ruptured spontaneously leaving raw areas. The history and physical examination suggested epidermolysis bullosa simplex and so, skin biopsy was done to confirm the diagnosis. On confirmation, patient’s parents were counselled about the disease and its management. <strong></strong></p>

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