Primary somatomedin deficiency: Case report
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چکیده
منابع مشابه
Primary somatomedin deficiency. Case report.
Primary somatomedin deficiency: case report. A child presenting with the clinical features of hyposomatotropism but with high immunoreactive plasma growth hormone is described. During short-term administration of human growth hormone (HGH) his response with regard to fasting blood-glucose and free fatty acids, plasma-somatomedin, urinary excretion of calcium, nitrogen, and hydroxyproline was mi...
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Two sisters of Asian origin showed typical clinical and biochemical features of primary somatomedin C (SM-C) deficiency (Laron dwarfism). Abnormalities of SM-C binding proteins were observed, one sister lacking the high molecular weight (150 Kd) protein.
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1974
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.49.4.297