Familial idiopathic hypoparathyroidism and progressive sensorineural deafness.
Open Access
- 1 January 1986
- journal article
- research article
- Published by Tohoku University Medical Press in The Tohoku Journal of Experimental Medicine
- Vol. 148 (2) , 135-141
- https://doi.org/10.1620/tjem.148.135
Abstract
YUMITA, S., FURUKAWA, Y., SOHN, H.E., UNAKAMI, H., MIURA, R. and YOSHINAGA, K. Familial Idiopathic Hypoparathyroidism and Progressive Sensorineural Deafness. Tohoku J. exp. Med., 1986, 148 (2), 135-141 - Three cases from two families with idiopathic hypoparathyroidism and progressive sensorineural deafness are described. Cases 1 and 2 were siblings. Case 3 was one of four siblings from another family. All of them had both idiopathic hypoparathyroidism and progressive sensorineural hearing loss. There was no evidence to suggest involvement of autoimmune mechanism in these cases except for the associated Graves' hyperthyroidism in case 3. Human leukocyte antigen A9 and A11 were positive in both families. The sensorineural hearing loss was progressive even after the treatment for hypoparathyroidism. As the familial idiopathic hypoparathyroidism is a very rare entity, it is unlikely that this disease is associated with familial progressive sensorineural deafness by chance. The combination of these two diseases may compose a new syndrome.Keywords
This publication has 4 references indexed in Scilit:
- Vitamin D deficiency—a new cause of cochlear deafnessThe Journal of Laryngology & Otology, 1983
- Stimulation of 1,25-dihydroxyvitamin D production by parathyroid hormone and dibutyryl 3',5'-cyclic AMP in normal subjects,hypoparathyroidism and pseudohypoparathyroidism.The Tohoku Journal of Experimental Medicine, 1982
- Nephrogenous Cyclic Adenosine Monophosphate as a Parathyroid Function TestJournal of Clinical Investigation, 1977
- Familial nephrosis, nerve deafness, andhypoparathyroidismThe Journal of Pediatrics, 1977