Barakat Syndrome in a Child: An Uncommon Cause of Hypocalcemic Tetany – A Case Report with Review of Literature
Background: Barakat syndrome is a rare autosomal dominant disorder caused by mutations in the GATA3 gene, manifesting with a combination of hypoparathyroidism, sensorineural deafness, and renal dysplasia. Clinical Description: A 12-year-old girl presented with sudden onset carpopedal spasms associat...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-04-01
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| Series: | Indian Pediatrics Case Reports |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/ipcares.ipcares_247_24 |
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