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Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients
Laron’s syndrome (LS) is a rare genetic disorder characterized by insensitivity to growth hormone (GH). Up to the present time, over 70 mutations of GH receptor (GHR) gene have been identified leading to GH/insulin-like growth factor type 1 (IGF1) signaling pathway defect. The number of LS patients...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Sociedade Brasileira de Genética
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7197995/ https://www.ncbi.nlm.nih.gov/pubmed/31429861 http://dx.doi.org/10.1590/1678-4685-GMB-2018-0197 |