HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Renal Tubular Acidosis and Endocrine Abnormalities

Author:

Taslipinar Abdullah1,Kebapcilar Levent1,Kutlu Mustafa1,Sahin Mustafa1,Aydogdu Aydogan1,Uckaya Gokhan1,Azal Omer1,Bolu Erol1,Ibrahim Aydin Halil2

Affiliation:

1. Department of Internal Medicine, Division of Endocrinology and Metabolism, Gulhane Military Medical Faculty

2. Department of Internal Medicine Pediatrics, Division of Metabolism, Gulhane Military Medical Faculty

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference14 articles.

1. Renal tubular acidosis: developments in our understanding of the molecular basis

2. 2. Herrin TJ. Renal tubular acidosis. In: Pediatric Nephrology. 4th edn. Baratt TM, Avner ED, Harmon WE, Eds. Williams & Wilkins, Baltimore, 1999: 565-583.

3. 3. Buckalew VM Jr, Caruana RJ. The pathophysiology of distal (type 1) renal tubular acidosis. In: Renal Tubular Disorder: Pathophysiology, Diagnosis, and Management. Gonick HC, Buckalew VM Jr, Eds. Dekker, New York, 1985: 357-386.

4. Bone mineral density and histology in distal renal tubular acidosis

5. Fanconi’s syndrome and distal (Type 1) renal tubular acidosis in a patient with primary Sjögren’s syndrome with monoclonal gammopathy of undetermined significance

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