[CITATION][C] Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred
MP Whyte, VV Weldon - The Journal of Pediatrics, 1981 - Elsevier
MP Whyte, VV Weldon
The Journal of Pediatrics, 1981•ElsevierFigure. Hypocalcemia, hyperphosphatemia, undetectable immunoreactive parathyroid
hormone levels, and a phospha~ turic response to parathyroid extract established the
diagnosis of IH P in the propositi (VI-11 and V1-12) and in patients IV-22 and V-53. X-linked
recessive inheritance for hypoparathyroidism is strongly suggested by a history of seizures
during infancy in 16 boys, but no girls, throughout generations III to VI.
hormone levels, and a phospha~ turic response to parathyroid extract established the
diagnosis of IH P in the propositi (VI-11 and V1-12) and in patients IV-22 and V-53. X-linked
recessive inheritance for hypoparathyroidism is strongly suggested by a history of seizures
during infancy in 16 boys, but no girls, throughout generations III to VI.
Figure. Hypocalcemia, hyperphosphatemia, undetectable immunoreactive parathyroid hormone levels, and a phospha~ turic response to parathyroid extract established the diagnosis of IH P in the propositi (VI-11 and V1-12) and in patients IV-22 and V-53. X-linked recessive inheritance for hypoparathyroidism is strongly suggested by a history of seizures during infancy in 16 boys, but no girls, throughout generations III to VI.
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