scholarly journals Pretibial dystrophic epidermolysis bullosa pruriginosa: A rare case report in a child with low intelligent quotient

2016 ◽  
Vol 17 (1) ◽  
pp. 32
Author(s):  
B Vijaya ◽  
SR Narahari ◽  
Pallavi Deka ◽  
GV Manjunath
Keyword(s):  
Case Report ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Dystrophic Epidermolysis Bullosa ◽  
Rare Case Report ◽  
Intelligent Quotient

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

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

Empyema due to salmonella typhi in a diabetic patient: a rare case report

2011 ◽  
Vol 3 (6) ◽  
pp. 405-406
Author(s):  
Dr. Nale Swati S Dr. Nale Swati S ◽  
◽  
Dr.Ghadage Dnyaneshwari P ◽  
Bhore Arvind V
Keyword(s):  
Case Report ◽  
Diabetic Patient ◽  
Rare Case ◽  
Salmonella Typhi ◽  
Rare Case Report

An Uncommon Presentation of Polycythemia Vera as Ischemic Stroke—A Rare Case Report

2012 ◽  
Vol 3 (5) ◽  
pp. 455-457
Author(s):  
Dr .KOUSHIK GUDAVALLI ◽  
◽  
Dr .SHILPA CHIKATI ◽  
Dr .MOHAN RAO JAKKAMPUTI ◽  
Dr .KAMAL LOCHAN BEHERA ◽  
...  
Keyword(s):  
Ischemic Stroke ◽  
Case Report ◽  
Polycythemia Vera ◽  
Rare Case ◽  
Uncommon Presentation ◽  
Rare Case Report
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