Job’s Syndrome: A Rare Case Report

2020 ◽  
Vol 59 (4-5) ◽  
pp. 505-507
Author(s):  
S. Richa ◽  
Himani Bhasin ◽  
Bishnupriya Sahoo ◽  
Pankaj Abrol ◽  
Shashi Sharma
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Job’S Syndrome ◽  
Rare Case Report ◽  
Job's Syndrome

scholarly journals Hyper-immunoglobulin E (Job's syndrome): A rare case report

2017 ◽  
Vol 18 (1) ◽  
pp. 73
Author(s):  
Shubhankar Mishra ◽  
SunilK Agarwalla ◽  
Sadhana Panda ◽  
AshisK Patel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Immunoglobulin E ◽  
Job’S Syndrome ◽  
Rare Case Report ◽  
Job's Syndrome

JOB'S SYNDROME: A RARE CASE REPORT

2021 ◽  
pp. 34-35
Author(s):  
Eshwar Rajesh ◽  
Shakuntala T
Keyword(s):  
Case Report ◽  
Autosomal Recessive ◽  
Genetic Disorder ◽  
Elevated Serum ◽  
Deciduous Teeth ◽  
Job’S Syndrome ◽  
Rare Case Report ◽  
Tissue Abnormalities ◽  
Job's Syndrome ◽  
Shed Light

Hyper IgE Syndrome (HIES) or Job's Syndrome is a complex primary immunodeciency disorder characterized by elevated serum IgE levels, recurrent skin rashes, eosinophilia, skeletal and connective tissue abnormalities. The patients also exhibit features of specic facies, retention of deciduous teeth and susceptibility to infections. HIES is a rare genetic disorder where some cases are inherited as autosomal dominant or autosomal recessive but most cases are supposedly sporadic. Hereby we present a case of 12-year-old male child admitted in the hospital with complaints of fever, skin rashes, intermittent abdominal pain and generalised lymphadenopathy. As there is no denite cure for HIES, the approach was directed towards conservative management. Due to the extreme paucity of reported cases in literature, this case report can help shed light on a syndrome of such rarity.

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

Recurrent and Metastatic Dermatofibrosarcomaprotuberans (DfSP): A Relatively Rare Case Report

2012 ◽  
Vol 3 (5) ◽  
pp. 413-414
Author(s):  
Dr. Prashant Kumbhaj ◽  
◽  
Dr. Rameshwaram Sharma ◽  
Dr. Aseemrai bhatnagar ◽  
Dr. Peeyush Kumar Saini
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report
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