Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency

Background and Objectives: Combined pituitary hormone deficiency (CPHD) is a rare heterogeneous disease. It is characterized by the deficiency of growth hormone (GH) and shortage of at least one or more other hormones of the pituitary gland including thyroid-stimulating hormone (TSH), luteinizing ho...

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Detalles Bibliográficos
Autores principales: Almatrafi, Ahmed M., Hibshi, Ali M., Basit, Sulman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052823/
https://www.ncbi.nlm.nih.gov/pubmed/36984475
http://dx.doi.org/10.3390/medicina59030474

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052823/
https://www.ncbi.nlm.nih.gov/pubmed/36984475
http://dx.doi.org/10.3390/medicina59030474

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