scholarly journals Extensive nephroureteric calcification presenting with renal failure: A rare case report

2015 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
AnupS Desai ◽  
SiddangoudaB Patil ◽  
VinayS Kundargi ◽  
AshokN Biradar
Keyword(s):  
Renal Failure ◽  
Case Report ◽  
Rare Case ◽  
Rare Case Report

Coexistence of chronic renal failure, hashimoto thyroiditis and idiopathic hypoparathyroidism: a rare case report

Renal Failure ◽  
2014 ◽  
Vol 36 (3) ◽  
pp. 441-443
Author(s):  
Saliha Yildiz ◽  
Yasemin Soyoral ◽  
Davut Demirkiran ◽  
Mustafa Ozturk
Keyword(s):  
Renal Failure ◽  
Case Report ◽  
Chronic Renal Failure ◽  
Rare Case ◽  
Hashimoto Thyroiditis ◽  
Rare Case Report

scholarly journals Meckel Gruber Syndrome: a rare case report

2017 ◽  
Vol 5 (1) ◽  
pp. 262
Author(s):  
Manish Verma ◽  
Shruti Sharma ◽  
Kiran Suthar ◽  
Beena Thada
Keyword(s):  
Renal Failure ◽  
Case Report ◽  
Rare Case ◽  
Autosomal Recessive ◽  
Pulmonary Hypoplasia ◽  
Autosomal Recessive Disorder ◽  
Polycystic Kidneys ◽  
Rare Autosomal Recessive Disorder ◽  
Live Births ◽  
Rare Case Report

Meckel gruber syndrome or dysencephalia splanchnocystica, is a rare autosomal recessive disorder caused by failure of mesodermal induction. Worldwide incidence of MGS is 1 per 13,500-140,000 live births. It is characterized by triad of occipital Meningoencephalocele, polycystic kidneys and post-axial polydactyly. Most fetuses affected with this syndrome die before birth due to oligohydramnios, renal failure or pulmonary hypoplasia. We report a rare case of MGS who delivered live at birth with classical features.

Paediatric bladder neurofibroma on bilateral ureterostomy: rare case report—strategic management

2021 ◽  
Vol 14 (2) ◽  
pp. e238296
Author(s):  
Pavai Arunachalam ◽  
Sudipta Sen ◽  
Dhanashree Balaji ◽  
Cenita J Sam
Keyword(s):  
Renal Failure ◽  
Case Report ◽  
Strategic Management ◽  
Rare Case ◽  
Plexiform Neurofibroma ◽  
Total Excision ◽  
Rare Case Report ◽  
Partial Excision

Urogenital involvement in neurofibromatosis is extremely rare and thus is less documented. Herein, we discuss a 11-year-old boy who was referred with a diagnosis of neurofibroma bladder on bilateral flank ureterostomy with mild renal failure. A diagnosis of neurofibroma of the bladder with ureterohydronephrosis had been made and partial excision had been attempted, followed by bilateral ureterostomy because of increasing ureterohydronephrosis. He was 13 years and wanted to be dry as he wanted to go to school. With the plan of attaining dryness with stable upper tracts, he was posted for surgery. Near-total excision followed by a sigmoid conduit was performed. The biopsy was reported as plexiform neurofibroma and is on regular follow-up, dry on a stoma bag with stable renal parameters.

Fenofibrate-induced rhabdomyolysis in a patient with chronic renal failure due to nephrotic syndrome: A rare case report

2012 ◽  
Vol 45 (1-2) ◽  
pp. 162-164 ◽  
Author(s):  
Fatih Mehmet Erdur ◽  
Yasemin Usul Soyoral ◽  
Habib Emre ◽  
Huseyin Begenik ◽  
Esra Turan Canbaz ◽  
...  
Keyword(s):  
Renal Failure ◽  
Nephrotic Syndrome ◽  
Case Report ◽  
Chronic Renal Failure ◽  
Rare Case ◽  
Rare Case Report

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
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