Klinefelter Syndrome with Short Stature
A case of Klinefelter syndrome (KS) is presented where the height SD score was -2.0 and the bone age was 7.0yr when the chronological age was 11.0yr. The patienthad a normal response to a GH stimulation test, but his mean GH secretion during sleep, the first morning-voided urinary GH and the plasma...
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Veröffentlicht in: | Clinical Pediatric Endocrinology 1993, Vol.2(Supple2), pp.99-101 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A case of Klinefelter syndrome (KS) is presented where the height SD score was -2.0 and the bone age was 7.0yr when the chronological age was 11.0yr. The patienthad a normal response to a GH stimulation test, but his mean GH secretion during sleep, the first morning-voided urinary GH and the plasma somatomedin-C (Sm-C) levels were abnormally low. It is likely that the patient's short stature resulted from GH neurosecretory dysfunction (GHND). |
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ISSN: | 0918-5739 1347-7358 |
DOI: | 10.1297/cpe.2.Supple2_99 |