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http://dx.doi.org/10.12655/KADH.2019.15.1.45

DENTAL TREATMENT OF A PATIENT WITH BARTTER SYNDROME: CASE REPORT  

Kim, Minji (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Song, Ji-Soo (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Shin, Teo Jeon (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Hyun, Hong-Keun (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Kim, Young-Jae (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Kim, Jung-Wook (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Lee, Sang-Hoon (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Jang, Ki-Taeg (Department of Pediatric Dentistry, School of Dentistry, Seoul National University)
Publication Information
The Journal of Korea Assosiation for Disability and Oral Health / v.15, no.1, 2019 , pp. 45-49 More about this Journal
Abstract
Bartter syndrome is an inherited renal tubular disorder characterized by hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia, hyperprostaglandinism, and normal blood pressure. Bartter syndrome is classified by neonatal and classic type. Clinical manifestation of Bartter syndrome considered in dental treatment include tendency to dehydration, vomiting and erosion, attrition and abrasion of the teeth. A 2-year-4 month old boy with Bartter syndrome type III was referred to the Seoul National University Dental Hospital for dental evaluation and treatment. He showed hypokalemic hypochloremic metabolic alkalosis and had been treated with indomethacin and potassium chloride. He had hypocalcified teeth with or without multisurface caries lesions in all dentition and the erosion of maxillary teeth was detected. Dental procedure under general anesthesia was scheduled due to multiple caries and his medical condition. The dental procedure was successfully performed. This case suggests that electrolyte imbalances need to be treated prior to dental treatment and complete coverage restoration is necessary to protect the eroded teeth. An appropriate management plan for the patients with Bartter syndrome should include considerations of the need for close interaction with the pediatrician for pre- and post-operative care. General anesthesia may be recommendable to manage the patients having multiple caries with Bartter syndrome.
Keywords
Bartter syndrome; Dental treatment; General anesthesia;
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1 Hebert SC: Bartter syndrome. Current opinion in nephrology and hypertension 12(5): 527-532, 2003.   DOI
2 Higa K, et al: Anesthetic management of a patient with Bartter's syndrome. Journal of clinical anesthesia 5(4): 321-324, 1993.   DOI
3 Kannan S, et al: Anaesthetic management of a child with Bartter's syndrome. Canadian journal of anaesthesia 42(9):808, 1995.   DOI
4 Martelli-Junior H, et al: Typical features of amelogenesis imperfecta in two patients with Bartter's syndrome. Nephron Extra 2(1): 319-325, 2012.   DOI
5 Martelli-Junior H, et al: Amelogenesis imperfecta and nephrocalcinosis syndrome: a case report and review of the literature. Nephron Physiology 118(3): p62-p65, 2011.   DOI
6 Shaer AJ: Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes. The American journal of the medical sciences 322(6): 316-332, 2001.   DOI
7 Amirlak I, Dawson K: Bartter syndrome: an overview. Qjm 93(4):207-215, 2000.   DOI
8 Gozneli R, et al: Effects of Bartter's syndrome on dentition and dental treatment: A clinical report. The Journal of prosthetic dentistry 93(6): 522-525, 2005.   DOI
9 Bettinelli A, et al: Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes. The Journal of pediatrics 120(1):38-43, 1992.   DOI
10 Fremont OT, Chan JC: Understanding Bartter syndrome and Gitelman syndrome. World Journal of Pediatrics 8(1): 25-30, 2012.   DOI