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- W2077880387 abstract "Six children are described with idiopathic gigantism. All but one were large at birth. One was a congenital giant, and the others had accelerated growth in early years of life. Two of them were concordant monozygotic twins. One patient underwent a normal a dolescent spurt and eventually achieved gigantic adult size when growth in height ceased. Macrocrania, large extremities, large hands and feet, and evidence of cerebral dysfunction were present in all; these cases appear to fit the syndrome of cerebral gigantism. Serum human growth hormone and insulin assays during glucose tolerance tests were normal except in one patient who had a paradoxical rise in his serum growth hormone level." @default.
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- W2077880387 date "1967-06-01" @default.
- W2077880387 modified "2023-09-23" @default.
- W2077880387 title "Cerebral gigantism: Endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who achieved adult gigantic size" @default.
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- W2077880387 doi "https://doi.org/10.1016/s0022-3476(67)80263-4" @default.
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