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Favorable Growth Hormone Treatment Response in a Young Boy with Achondroplasia
BACKGROUND: Achondroplasia is a skeletal dysplasia, the most common cause of rhizomelic dwarfism. CASE PRESENTATION: This is a ten year old boy who was first diagnosed prenatally. He had a mutation c1138G>A in the gene FGFR3 in a heterozygotic constellation. His IGF1 and IGFBP3 levels were normal...
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| Publié dans: | Med Arch |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
AVICENA, d.o.o., Sarajevo
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4851542/ https://ncbi.nlm.nih.gov/pubmed/27147792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5455/medarh.2016.70.148-150 |
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