| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1081127 | Journal of Adolescent Health | 2006 | 4 Pages |
Abstract
This is a clinical presentation of a healthy 12-year-old African-American male who had symptomatic hypocalcemia during a growth spurt that resolved after reaching a stable height. He had clinical findings consistent with Pseudohypoparathyroidism (PHP) with hypocalcemia, hyperphospatemia, and increased parathyroid hormone (PTH) concentration. We hypothesize that his family might have a hitherto unreported autosomal dominant PHP-Ib that may or may not be linked to the GNAS locus.
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Authors
Kathryn L. D.O., Erawati V. M.D.,
