Cargando…
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
Combined pituitary hormone deficiency (CPHD) is not a rare disorder, with a frequency of approximately 1 case per 4,000 live births. However, in most cases, a genetic diagnosis is not available. Furthermore, the diagnosis is challenging because no clear correlation exists between the pituitary hormo...
Autores principales: | Bando, Hironori, Urai, Shin, Kanie, Keitaro, Sasaki, Yuriko, Yamamoto, Masaaki, Fukuoka, Hidenori, Iguchi, Genzo, Camper, Sally A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551393/ https://www.ncbi.nlm.nih.gov/pubmed/36237189 http://dx.doi.org/10.3389/fendo.2022.1008306 |
Ejemplares similares
-
ODP329 Long-term Effect of Daily Growth Hormone Replacement Therapy on Glucose Tolerance in Adult growth Hormone Deficiency
por: Bando, Hironori, et al.
Publicado: (2022) -
Mechanistic insights into immune checkpoint inhibitor-related hypophysitis: a form of paraneoplastic syndrome
por: Kanie, Keitaro, et al.
Publicado: (2021) -
Case report: Late middle-aged features of FAM111A variant, Kenny–Caffey syndrome type 2-suggestive symptoms during a long follow-up
por: Ohmachi, Yuka, et al.
Publicado: (2023) -
Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody
por: Urai, Shin, et al.
Publicado: (2023) -
SAT141 A Case Of Non-islet Cell Tumor Hypoglycemia Which Was Ameliorated By Pazopanib Treatment
por: Yamamoto, Naoki, et al.
Publicado: (2023)