Literature DB >> 26156834

Vitamin D deficiency in a patient with HDR syndrome.

Ifigenia Kostoglou-Athanassiou1, Dimitrios Stefanopoulos1, Areti Karfi1, Panagiotis Athanassiou2.   

Abstract

The case of a patient with clinical symptoms, laboratory and imaging findings of hypoparathyroidism, sensorineural deafness, renal dysplasia HDR, or Barakat syndrome (hypoparathyroidism, deafness, renal dysplasia), and vitamin D deficiency, is presented. A Caucasian man aged 51 years with a history of chronic hypocalcaemia since childhood, was admitted with hypertonia of the body and extremities, and loss of consciousness. On admission, he was found to have severe hypocalcaemia, hyperphosphataemia, severe hypoparathyroidism, low serum magnesium and mild renal insufficiency. Calcium gluconate was administered intravenously supplemented with magnesium, and the patient recovered consciousness while clinical and laboratory findings improved. Evaluation revealed left renal aplasia and sensorineural deafness affecting both ears. Vitamin D deficiency was also present. He was given calcium and vitamin D supplements orally, and the hypocalcaemia was corrected. This case is described as it is an extremely rare case of HDR syndrome with concurrent vitamin D deficiency. 2015 BMJ Publishing Group Ltd.

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Year:  2015        PMID: 26156834      PMCID: PMC4499749          DOI: 10.1136/bcr-2014-208290

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  12 in total

1.  Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia.

Authors:  R W Bilous; G Murty; D B Parkinson; R V Thakker; M G Coulthard; J Burn; D Mathias; P Kendall-Taylor
Journal:  N Engl J Med       Date:  1992-10-08       Impact factor: 91.245

2.  Familial nephrosis, nerve deafness, and hypoparathyroidism.

Authors:  A Y Barakat; J B D'Albora; M M Martin; P A Jose
Journal:  J Pediatr       Date:  1977-07       Impact factor: 4.406

3.  Molecular and clinical characterization of patients with overlapping 10p deletions.

Authors:  Anna Lindstrand; Helena Malmgren; Annapia Verri; Elisa Benetti; Maud Eriksson; Ann Nordgren; Britt-Marie Anderlid; Irina Golovleva; Jacqueline Schoumans; Elisabeth Blennow
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

4.  Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

Authors:  Alireza Zahirieh; M Andrew Nesbit; Asif Ali; Kairong Wang; Ning He; Maria Stangou; Gerasimos Bamichas; Kostas Sombolos; Rajesh V Thakker; York Pei
Journal:  J Clin Endocrinol Metab       Date:  2005-02-10       Impact factor: 5.958

5.  Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia.

Authors:  Amar Al-Shibli; Ibrahim Al Attrach; Patrick J Willems
Journal:  Pediatr Nephrol       Date:  2011-03-12       Impact factor: 3.714

6.  HDR syndrome (hypoparathyroidism, sensorineural deafness and renal disease) accompanied by renal tubular acidosis and endocrine abnormalities.

Authors:  Abdullah Taslipinar; Levent Kebapcilar; Mustafa Kutlu; Mustafa Sahin; Aydogan Aydogdu; Gokhan Uckaya; Omer Azal; Erol Bolu; Halil Ibrahim Aydin
Journal:  Intern Med       Date:  2008-06-02       Impact factor: 1.271

7.  Case of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome associated with nephrocalcinosis and distal renal tubular acidosis.

Authors:  Yuji Kato; Naoki Wada; Atsushi Numata; Hidehiro Kakizaki
Journal:  Int J Urol       Date:  2007-05       Impact factor: 3.369

8.  The syndrome of hypoparathyroidism, deafness, and renal anomalies.

Authors:  Jagriti Upadhyay; Devin W Steenkamp; Jeff M Milunsky
Journal:  Endocr Pract       Date:  2013 Nov-Dec       Impact factor: 3.443

9.  Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

Authors:  M Andrew Nesbit; Michael R Bowl; Brian Harding; Asif Ali; Alejandro Ayala; Carol Crowe; Angus Dobbie; Geeta Hampson; Ian Holdaway; Michael A Levine; Robert McWilliams; Susan Rigden; Julian Sampson; Andrew J Williams; Rajesh V Thakker
Journal:  J Biol Chem       Date:  2004-02-24       Impact factor: 5.157

10.  Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome.

Authors:  Marjolein A J van Looij; Hanne Meijers-Heijboer; Rolf Beetz; Rajesh V Thakker; Paul T Christie; Lou W Feenstra; Bert G A van Zanten
Journal:  Audiol Neurootol       Date:  2006-09-21       Impact factor: 1.854

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