Severe primary hyperparathyroidism in a 3-day-old neonate
Neonatal severe primary hyperparathyroidism (NSHPT) is a rare and life-threatening autosomal recessive genetic disorder caused by a wide range of inactivating mutations in Calcium sensing receptors. We introduced a three-day-old neonate with poor feeding, failure to thrive, and lethargy. The laborat...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2021-01-01
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| Series: | Journal of Pediatric Surgery Case Reports |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2213576620303535 |