Extrapyramidal Symptoms and Advanced Calcification of the Basal Ganglia in a Patient with Autosomal Dominant Hypocalcemia

Author:

Kurozumi Akira1,Okada Yosuke1,Arao Tadashi1,Endou Itsuro2,Matsumoto Toshio2,Tanaka Yoshiya1

Affiliation:

1. The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, Japan

2. Institute of Health Biosciences, University of Tokushima, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference22 articles.

1. 1. Fukumoto S, Namba N, Ozono K, et al. Causes and differential diagnosis of hypocalcemia-recommendation proposed by expert panel supported by Ministry of Health, Labour and Welfare, Japan. Endocr J 55: 787-794, 2008.

2. 2. Lienhardt A, Bai M, Lagarde JP, et al. Activating mutations of the calcium-sensing receptor: management of hypocalcemia. J Clin Endocrinol Metab 86: 5313-5323, 2001.

3. 3. Gunn IR, Gaffney D. Clinical and laboratory features of calcium-sensing receptor disorders: a systematic review. Ann Clin Biochem 41: 441-458, 2004.

4. 4. Pllak MR, Brown EM, Estep HL, et al. Autosomal dominant hypocalcemia caused by a Ca2+-sensing receptor gene mutation. Nat Genet 8: 303-307, 1994.

5. 5. Mittelman SD, Hendy GN, Fefferman RA, et al. A hypocalcemic child with a novel activating mutation of the calcium-sensing receptor gene: successful treatment with recombinant human parathyroid hormone. J Clin Endocrinol Metab 91: 2474-2479, 2006.

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