Acromegaly
What's New
Last Posted: Mar 26, 2024
- Genetic diagnosis in acromegaly and gigantism: From research to clinical practice.
Claudia Ramírez-Rentería et al. Best Pract Res Clin Endocrinol Metab 2024 101892 - Machine learning-based algorithms applied to drug prescriptions and other healthcare services in the Sicilian claims database to identify acromegaly as a model for the earlier diagnosis of rare diseases.
Salvatore Crisafulli et al. Sci Rep 2024 14(1) 6186 - FTO Gene Polymorphisms and Their Roles in Acromegaly.
Aleksandra Jawiarczyk-Przyby?owska, et al. International journal of molecular sciences 2023 0 (13) - Erectile function and androgen and estrogen beta receptor gene polymorphisms in acromegalic men.
F Pallotti, et al. Journal of endocrinological investigation 2023 0 - Increased prevalence of proliferative retinopathy in patients with acromegaly.
Wu Tzu-En, et al. Journal of the Chinese Medical Association : JCMA 2017 0 (3) 230-235 - GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly.
Ferraù F, et al. Journal of endocrinological investigation 2018 0 (7) 825-831 - Screening for germline KCNQ1 and KCNE2 mutations in a set of somatotropinoma patients.
Iivonen Anna-Pauliina, et al. Endocrine connections 2018 0 (5) 645-652 - Germline mutations of aryl hydrocarbon receptor-interacting protein (AIP) gene and somatostatin receptor 1-5 and AIP immunostaining in patients with sporadic acromegaly with poor versus good response to somatostatin analogues.
Ozkaya Hande Mefkure, et al. Pituitary 2018 0 (4) 335-346 - Exon 3-deleted growth hormone receptor isoform is not related to worse bone mineral density or microarchitecture or to increased fracture risk in acromegaly.
Pontes J, et al. Journal of endocrinological investigation 2019 0 (2) 163-171 - Hepatic steatosis in patients with acromegaly.
Koutsou-Tassopoulou Andreani, et al. Endocrinology, diabetes & metabolism 2019 0 (4) e00090
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 21, 2024
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