| Autor: |
Tauber MT; Service d'Endocrinologie pédiatrique, CHU Purpan, Toulouse, France. tauber.mt@chu.toulouse.fr, Porra V, Dastot F, Molinas C, Amselem S, Cholin S, Rochiccioli P, Bieth E |
| Jazyk: |
angličtina |
| Zdroj: |
Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society [Growth Horm IGF Res] 1998 Jun; Vol. 8 (3), pp. 211-6. |
| DOI: |
10.1016/s1096-6374(98)80113-5 |
| Abstrakt: |
Besides complete GH insensitivity syndrome (GHIS) described by Laron, clinical and molecular evidences have accumulated concerning partial GHIS. We studied GH receptor (GHR) gene in children who show poor response to GH treatment and detected a patient with a heterozygous mutation in exon 7 leading to the Y222H substitution. This missense mutation, located in the YGEFS motif of the GHR equivalent to the WSXWS motif highly conserved throughout all members of the cytokine receptor family, has not been described so far. Although we cannot conclude on the deleterious effect of this mutation, there are several lines of evidence suggesting that it could account for the partial GH insensitivity: (i) hormonal data including IGF-I generation test; (ii) molecular data - no other mutation was identified in the coding sequence, the father who has the same mutation is short, the brother did not inherit the mutated allele and was of normal height. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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