Neonatal primary hyperparathyroidism with autosomal dominant inheritance
Spiegel, A.M.; Harrison, H.E.; Marx, S.J.; Brown, E.M.; Aurbach, G.D.
Journal of Pediatrics 90(2): 269-272
1977
ISSN/ISBN: 0022-3476 PMID: 830920 Document Number: 115446
Primary hyperthyroidism is diagnosed in 15 clinical cases and is characterized by anorexia, hypotonia, bony deminerialization, hypercalcemia and parathyroid hyperplasia. The disease is inherited as a autosomal dominant trait and is discussed in terms of its diagnosis and therapy.
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