Presentation and clinical progression of pseudohypoparathyroidism with multi-hormone resistance and Albright hereditary osteodystrophy: A case series

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Anthropometric and biochemical features were retrospectively evaluated in 12 patients with pseudohypoparathyroidism, Albright hereditary osteodystrophy, and multi-hormone resistance. Hypothyroidism and subcutaneous calcifications were presenting features in younger children. Temporal trends in stimulatory hormone resistance included early thyroid-stimulating hormone elevation and progression from parathyroid hormone elevation to hyperphosphatemia and hypocalcemia.

Original languageEnglish (US)
Pages (from-to)877-880.e1
JournalJournal of Pediatrics
Issue number6
StatePublished - Dec 2006


ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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