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Journal of Clinical Endocrinology & Metabolism, Vol 55, 1020-1022, Copyright © 1982 by Endocrine Society


ARTICLES

Vitamin D resistant rickets with alopecia: cultured skin fibroblasts exhibit defective cytoplasmic receptors and unresponsiveness to 1,25(OH)2D3

D Feldman, T Chen, C Cone, M Hirst, S Shani, A Benderli and Z Hochberg

A new case of vitamin D dependent rickets (Type II) with alopecia in a 5 yr old child is reported. Skin fibroblasts were propagated in culture and analyzed for cytoplasmic 1,25(OH)2D3 receptors. The rachitic cells failed to exhibit specific, high-affinity binding sites by either Scatchard analysis or sucrose density gradient. Furthermore, a rise in 24-hydroxylase activity could not be elicited following incubation of the rachitig cells with 1,25(OH)2D3. Fibroblasts from a non-rachitic child examined in parallel experiments demonstrated high affinity binding sites (Kd = 0.1 nM, Nmax = 33 fmol/100 micrograms DNA) and the induction of 24-hydroxylase activity. The molecular basis of the unresponsiveness of the cells from the rachitic child appears to be due to defective or absent 1,25(OH)2D3 receptors.


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M. Hughes, P. Malloy, D. Kieback, R. Kesterson, J. Pike, D Feldman, and B. O'Malley
Point mutations in the human vitamin D receptor gene associated with hypocalcemic rickets
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J. Pike, S Dokoh, M. Haussler, U. Liberman, S. Marx, and C Eil
Vitamin D3--resistant fibroblasts have immunoassayable 1,25-dihydroxyvitamin D3 receptors
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