Učitavanje...
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...
Spremljeno u:
| Izdano u: | Med Arch |
|---|---|
| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
AVICENA, d.o.o., Sarajevo
2016
|
| Teme: | |
| Online pristup: | 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 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|