Saudi Journal of Kidney Diseases and Transplantation

CASE REPORT
Year
: 2008  |  Volume : 19  |  Issue : 6  |  Page : 964--968

Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor


Murugesan Ram Prabahar, Manish Jain, Venkatraman Chandrasekaran, Elayaperumal Indhumathi, Periasamy Soundararajan 
 Department of Nephrology, Sri Ramachandra Medical College, Sri Ramachandra University, Chennai, Tamilnadu, India

Correspondence Address:
Murugesan Ram Prabahar
Department of Nephrology, Sri Ramachandra Medical College, Sri Ramachandra University, Chennai-116, Tamilnadu
India

Thalassemia is a hereditary anemia resulting from defect in hemoglobin production. Beta thalassemia is due to impaired production of beta globin chains, leading to a relative excess of alpha globin chains. The term beta thalassemia minor is used to describe heterozygotes, who carry one normal beta globin allele and one beta thalassemic allele. The vast majority of these patients are asymptomatic. However, a variety of renal tubular abnormalities including hypercalciuria, hypo­magnesemia with renal magnesium wasting, decreased tubular absorption of phosphorus, hypo­uricemia with renal uric acid wasting, renal glycosuria and tubular proteinuria have been described even in patients with beta thalassemia minor. We here in report a 24-year old female patient who was found to have thalassemia minor and nephrocalcinosis with evidence of renal tubular dysfunction. Investigations revealed normal renal function, hypercalciuria, reduced tubular reabsorption of phos­phorus, hypomagnesemia and renal magnesium wasting. Screening for aminoaciduria was found to be negative. An acid loading test revealed normal urinary acidification. Ultrasonogram of the abdomen revealed nephrocalcinosis and splenomegaly. Detailed work up for anemia showed normal white cell and platelet count while peripheral smear showed microcytic hypochromic anemia with few target cells. Hemoglobin electrophoresis revealed hemoglobin A of 92%, hemoglobin A2 of 6.2% and hemo­globin F of 1.8% consistent with beta thalassemia minor. Her parental screening was normal. A diag­nosis of beta thalassemia minor with renal tubular dysfunction was made and the patient was started on thiazide diuretics to reduce hypercalciuria and advised regular follow-up.


How to cite this article:
Prabahar MR, Jain M, Chandrasekaran V, Indhumathi E, Soundararajan P. Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor.Saudi J Kidney Dis Transpl 2008;19:964-968


How to cite this URL:
Prabahar MR, Jain M, Chandrasekaran V, Indhumathi E, Soundararajan P. Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor. Saudi J Kidney Dis Transpl [serial online] 2008 [cited 2021 Jan 23 ];19:964-968
Available from: https://www.sjkdt.org/article.asp?issn=1319-2442;year=2008;volume=19;issue=6;spage=964;epage=968;aulast=Prabahar;type=0