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An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene.
Takeuchi, Takako; Yoto, Yuko; Tsugawa, Takeshi; Kamasaki, Hotaka; Kondo, Atsushi; Ogino, Jiro; Hasegawa, Tadashi; Yama, Naoya; Anan, Sawa; Uchino, Shinya; Ishikawa, Aki; Sakurai, Akihiro; Tsutsumi, Hiroyuki.
Affiliation
  • Takeuchi T; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Yoto Y; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Tsugawa T; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Kamasaki H; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Kondo A; Department of Otolaryngology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Ogino J; Department of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Hasegawa T; Department of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Yama N; Department of Radiology Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Anan S; Department of Pediatrics, Kinikyo Fushiko Jujo Clinic, Sapporo, Japan.
  • Uchino S; Department of Surgery, Noguchi Thyroid Clinic and Hospital Foundation, Beppu, Japan.
  • Ishikawa A; Department of Medical Genetics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Sakurai A; Department of Medical Genetics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Tsutsumi H; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
Clin Pediatr Endocrinol ; 24(4): 185-9, 2015 Oct.
Article in En | MEDLINE | ID: mdl-26568659
ABSTRACT
A 13-yr-old boy who complained of persistent nausea, vomiting and weight loss had hypercalcemia and an elevated intact PTH level. Computed tomography confirmed two tumors in the thyroid gland. The tumors were surgically removed and pathologically confirmed as parathyroid adenoma. Because his maternal aunt and grandmother both had histories of parathyroid tumors, genetic investigation was undertaken for him, and a germline frameshift mutation of the CDC73 gene was identified. CDC73 gene analysis should be done on individuals who are at risk of familial hyperparathyroidism, including those who are asymptomatic, and they should be followed for potential primary hyperparathyroidism and associated disorders including resultant parathyroid carcinoma.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Clin Pediatr Endocrinol Year: 2015 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Clin Pediatr Endocrinol Year: 2015 Document type: Article Affiliation country: