Clinical challenges in the management of isolated GH deficiency type IA in adulthood

Isolated GH deficiency type IA (IGHDIA) is an infrequent cause of severe congenital GHD, often managed by pediatric endocrinologists, and hence few cases in adulthood have been reported. Herein, we describe the clinical status of a 56-year-old male with IGHDIA due to a 6.7 kb deletion in GH1 gene th...

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Detalles Bibliográficos
Autores principales: Casteràs, Anna, Kratzsch, Jürgen, Ferrández, Ángel, Zafón, Carles, Carrascosa, Antonio, Mesa, Jordi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2014
Materias:
Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965272/
https://www.ncbi.nlm.nih.gov/pubmed/24683479
http://dx.doi.org/10.1530/EDM-13-0057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965272/
https://www.ncbi.nlm.nih.gov/pubmed/24683479
http://dx.doi.org/10.1530/EDM-13-0057

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