A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene
We experienced a case of familial hypoparathyroidism with an autosomal dominant pattern of transmission and performed molecular analysis of the calcium-sensing receptor (CASR) gene. The patient was a female neonate, born by cesarean section at term because of breech presentation. Her mother had bee...
| Main Authors: | , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
The Japanese Society for Pediatric Endocrinology
2008
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004876/ |