Abstract
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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- Eshet R., Laron Z., Pertzelan A., Arnon R., Dintzman M. Defect of human growth hormone receptors in the liver of two patients with Laron-type dwarfism. Isr J Med Sci. 1984 Jan;20(1):8–11. [PubMed] [Google Scholar]
- Hill D. J., Crace C. J., Fowler L., Holder A. T., Milner R. D. Cultured fetal rat myoblasts release peptide growth factors which are immunologically and biologically similar to somatomedin. J Cell Physiol. 1984 Jun;119(3):349–358. doi: 10.1002/jcp.1041190314. [DOI] [PubMed] [Google Scholar]
- Laron Z., Pertzelan A., Mannheimer S. Genetic pituitary dwarfism with high serum concentation of growth hormone--a new inborn error of metabolism? Isr J Med Sci. 1966 Mar-Apr;2(2):152–155. [PubMed] [Google Scholar]
- Pertzelan A., Adam A., Laron Z. Genetic aspects of pituitary dwarfism due to absence or biological inactivity of growth hormone. Isr J Med Sci. 1968 Jul-Aug;4(4):895–900. [PubMed] [Google Scholar]
- Wilkins J. R., D'Ercole A. J. Affinity-labeled plasma somatomedin-C/insulinlike growth factor I binding proteins. Evidence of growth hormone dependence and subunit structure. J Clin Invest. 1985 Apr;75(4):1350–1358. doi: 10.1172/JCI111836. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van den Brande J. L., du Caju M. V., Visser H. K., Schopman W., Hackeng W. H., Degenhart H. J. Primary somatomedin deficiency. Case report. Arch Dis Child. 1974 Apr;49(4):297–304. doi: 10.1136/adc.49.4.297. [DOI] [PMC free article] [PubMed] [Google Scholar]