Distal Rta Type I In Beta Thalassemia Trait With Rachitic Manifestation: A Case Report

Journal Title: IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) - Year 2018, Vol 17, Issue 11

Abstract

Beta thalassemia trait is a variant of beta thalassemia, which is a heterozygous state with features of mild anaemia, hypochromic microcytic red cells and elevated HbA2.Distal renal tubular acidosis (type I RTA) is an important cause of rachitic deformities, failure to thrive and hypokalemia.It ischaracterised by persistent severe metabolic acidosis. The proximal tubular reabsorption of bicarbonate is normal. Persistant acidosis and hypercalciuria leads to nephrocalcinosis.

Authors and Affiliations

Dr Antony Kisku, Dr Kiran Kumar M N

Keywords

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  • EP ID EP409185
  • DOI 10.9790/0853-1711033538.
  • Views 89
  • Downloads 0

How To Cite

Dr Antony Kisku, Dr Kiran Kumar M N (2018). Distal Rta Type I In Beta Thalassemia Trait With Rachitic Manifestation: A Case Report. IOSR Journal of Dental and Medical Sciences (IOSR-JDMS), 17(11), 35-38. https://europub.co.uk/articles/-A-409185