HDR Syndrome Accompanying Type 1 Diabetes Mellitus and Hypopituitarism. (16th May 2019)

• Record Type: Journal Article
• Authors: Can, Mustafa; Karakurt, Feridun; Kocabas, Muhammed; Cordan, İlker; Karakose, Melia; Kulaksızoglu, Mustafa
• Other Names: Isozaki Osamu Academic Editor.
• Is Part Of: Case reports in endocrinology. Volume 2019(2019)
• Publication Date: 2019-05-16
• Subjects: Endocrinology -- Periodicals; Endocrinology -- Case studies -- Periodicals; Endocrine glands -- Diseases -- Periodicals; Endocrinology; Endocrine System Diseases; Endocrine glands -- Diseases; Endocrinology; Electronic journals; Periodicals; Case studies; Periodicals; Case Reports; Fulltext; Internet Resources; Periodicals; 616.4
• DOI: 10.1155/2019/7276947
• Languages: English
• ISSNs: 2090-6501

Abstract

Abstract : HDR (Hypoparathyroidism, Deafness, and Renal Dysplasia) syndrome is an autosomal dominant disorder characterized by the triad of hypoparathyroidism, sensorineural deafness, and renal disease. Approximately 65% of patients with HDR syndrome have all three of these features, while others have different combinations of these features. We aimed to present a case with primary hypoparathyroidism, hearing loss, and nondiabetic chronic kidney disease and diagnosed as HDR syndrome while being followed up for type 1 diabetes mellitus and hypopituitarism.