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Annals of Pediatric Endocrinology & Metabolism ; : 129-132, 2019.
Article in English | WPRIM | ID: wpr-762600

ABSTRACT

We report a case of transient pseudohypoparathyroidism in a full-term newborn that presented at 20 hours of life with hypocalcemic seizures, hyperphosphatemia and raised parathormone levels. The diagnosis of pseudohypoparathyroidism was made according to biochemical investigations. The infant was treated with calcium supplementation and vitamin D analog therapy, and he remained stable and symptom-free with normal serum biochemistries during follow-up. We suggest that transient pseudohypoparathyroidism of the newborn (ntPHP) might be included among inactivating parathyroid hormone (PTH)/PTH-related protein signaling disorders as defined by the classification schema recently proposed by the European Pseudohypoparathyroidism Network. To the best of our knowledge, this is the first report in which the new classification has been applied to a case of ntPHP.


Subject(s)
Humans , Infant , Infant, Newborn , Calcium , Classification , Diagnosis , Follow-Up Studies , Hyperphosphatemia , Parathyroid Hormone , Precision Medicine , Pseudohypoparathyroidism , Seizures , Vitamin D
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