The insulin-like growth factor-I (IGF-I) generation test as an indicator of growth hormone status

Bessie E. Spiliotis, Theodore K. Alexandrides, Christoforos Karystianos, Pavlos Vassilakos, Zvi Zadik, Nikoleta M. Nikolakopoulou, George Nikiforidis, Nicholas G Beratis

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OBJECTIVE: The aim of the study was to evaluate the IGF-I generation test (IGF-I gen) as a possible indirect test of Growth Hormone (GH) secretory status. METHODS: Sixty-five GH deficient (GHD 1 and 2) and 86 control children were studied …

Pseudohypoparathyroidism type Ia and growth hormone deficiency. Growth hormone releasing hormone receptor defect?

Fotini Psychou, Polyxeni Nicolaidou, Helen Georgouli, Maria Maniati-Christidis, Catherine Dacou-Voutetakis
 

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We report a boy with pseudohypoparathyroidism (PHP), hypothyroidism and low growth hormone (GH) values with no response to growth hormone releasing hormone (GHRH). He presented at age 17 mo because of developmental delay. He had the typical features (short stature, obesity, round face, brachydactyly) of Albright’s hereditary osteodystrophy (AHO) …

PROP-1 gene mutations in a 63-year-old woman presenting with osteoporosis and hyperlipidaemia

Maria Andrikoula, Amalia Sertedaki, Sofia Andrikoula, Catherine Dacou-Voutetakis, Agathocles Tsatsoulis

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PROP-1 gene mutations have been reported as a cause of combined pituitary hormone deficiency. Physical and hormonal phenotypes of affected individuals are variable. We report a 63-year-old female who presented with osteoporosis

A prismatic case: A 31-year old man who did not miss his pituitary

Stefanie Petzold, Alexandra Keller, Eberhardt Keller, Christof Meigen, Wolfgang Hirsch, Jürgen Kratzsch, Wieland Kiess, Roland Pfäffle

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Combined pituitary hormone deficiency (CPHD) is a rare disorder resulting from impaired production of several pituitary hormones. This report describes the 30-year history of a patient who has apparently lived without a pituitary …