scholarly journals Ocular involvement in a case of dystrophic epidermolysis bullosa with conjunctival blistering without eyelid or corneal disease: A rare case report

2021 ◽  
Vol 59 (2) ◽  
pp. 169
Author(s):  
ShyamSundar Das Mohapatra ◽  
Dipankar Das ◽  
Harsha Bhattacharjee
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Ocular Involvement ◽  
Dystrophic Epidermolysis Bullosa ◽  
Corneal Disease ◽  
Rare Case Report

Hereditary Dystrophic Epidermolysis Bullosa A Rare Case Report

2015 ◽  
Vol 7 (2) ◽  
pp. 84-86
Author(s):  
Pallavi Urs ◽  
Shagun Sinha
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Diverse Group ◽  
Dystrophic Epidermolysis Bullosa ◽  
Tissue Separation ◽  
Rare Case Report ◽  
Oral Tissue ◽  
Care Practices

Abstract Epidermolysis bullosa (EB) is a diverse group of disorders characterized by blister formation with tissue separation occurring at variable depths in the skin and oral mucosa depending on the specific EB type. Oral tissue fragility and blistering is common to all EB types. However oral debilitation as a result of soft tissue scarring is primarily limited to the recessive dystrophic EB subtypes. Due to extreme mucosal fragility such patients are managed by modified dental care practices. This case report describes a rare case of recessive dystrophic EB. How to cite this article: Neena IE, Sinha S, Poornima P, Pallavi Urs. Hereditary Dystrophic Epidermolysis bullosa- A Rare Case Report. CODS J Dent 2015;7: 84-86

Primary Sjögren′s syndrome without ocular involvement: A rare case report

2014 ◽  
Vol 26 (1) ◽  
pp. 99
Author(s):  
Tushar Phulambrikar ◽  
Priya Pande ◽  
Siddharth Singh ◽  
Shali Magar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ocular Involvement ◽  
Rare Case Report

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>

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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