Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up

Costello syndrome (CS) is a rare member of the group of neuro-cardio-facio-cutaneous diseases known as RASopathies. CS involves characteristic dysmorphic craniofacial features, cardiac defects, and increased cancer susceptibility, depending on the heterozygous activating germline mutations in HRAS....

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Detalles Bibliográficos
Autores principales: Kizilcan Cetin, Sirmen, Siklar, Zeynep, Ozsu, Elif, Aycan, Zehra, Uyanik, Rukiye, Bilici, Meliha E., Ceran, Aysegul, Berberoglu, Merih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534522/
https://www.ncbi.nlm.nih.gov/pubmed/33088020
http://dx.doi.org/10.1297/cpe.29.195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534522/
https://www.ncbi.nlm.nih.gov/pubmed/33088020
http://dx.doi.org/10.1297/cpe.29.195

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