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Article in English | IMSEAR | ID: sea-95232

ABSTRACT

We report a case of Type 1 Renal Tubular Acidosis (RTA) in association with sensorineural deafness. Inherited Type 1 RTA is usually autosomal dominant, though there is a rarer recessive form associated with nerve deafness. Simple alkali replacement can correct the systemic metabolic defect, but does not appear to ameliorate hearing loss.


Subject(s)
Acidosis, Renal Tubular/complications , Buffers , Chelating Agents/therapeutic use , Child , Citrates/therapeutic use , Citric Acid/therapeutic use , Female , Follow-Up Studies , Hearing Loss, Sensorineural/complications , Humans , Rickets/diagnosis
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