Effect of Recombinant Human Growth Hormone Treatment in a Patient with Short Stature Associated with the Ring Chromosome 17 Syndrome

BACKGROUND: Ring chromosome 17 syndrome is a rare hereditary disorder whose prevalence is less than 1 : 1.000.000. We present a ten-year-old patient with ring chromosome 17 syndrome who had short stature and was treated with recombinant human growth hormone (rhGH). Case Report. A ten-year-old male s...

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Detalles Bibliográficos
Autores principales: Tempone Cardoso Penna, Gustavo, de Rezende Lelot, Gabriela, de Rezende Lelot, Ana Luiza, Greghi Hernandez, Juliana, Costa Figueiredo, Carolina, de Araujo Evangelista, Nara Michelle, Tonetto Fernandes, Vania de Fatima, de Paula Colares Neto, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545459/
https://www.ncbi.nlm.nih.gov/pubmed/37790920
http://dx.doi.org/10.1155/2023/6686511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545459/
https://www.ncbi.nlm.nih.gov/pubmed/37790920
http://dx.doi.org/10.1155/2023/6686511

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