Results 51 to 60 of about 13,861 (172)
Healthcare utilization and costs among patients with acromegaly in the United States
Aim: Recent evidence regarding the healthcare resource utilization (HCRU) and associated costs of acromegaly is limited. Materials & methods: This retrospective, cross-sectional administrative claims analysis (IQVIA Pharmetrics Plus) identified ...
Tiffany P Quock +8 more
doaj +1 more source
A male patient presented at the age of 30 with classic clinical features of acromegaly and was found to have elevated growth hormone levels, not suppressing during an oral glucose tolerance test.
Nikolaos Kyriakakis +6 more
doaj +1 more source
Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia
ABSTRACT Saul Wilson syndrome is an extremely rare genetic disorder caused by heterozygous de novo mutations in the COG4 gene. We report the first case from Saudi Arabia with previously unreported facial dysmorphic features, expanding the known phenotypic spectrum and emphasizing the importance of recognizing phenotypic variability in rare disorders.
Saad A. Bin Owaimer +4 more
wiley +1 more source
Clinical and economic burden among older adults with acromegaly in the United States
Aim: To compare healthcare resource utilization (HCRU) and costs between older adults with and without acromegaly. Materials & methods: Using 2017–2022 100% Medicare Research Identifiable Files, we identified beneficiaries (≥65 years) with prevalent ...
Tiffany P Quock +7 more
doaj +1 more source
Long‐standing growth hormone (GH) excess causes the skeletal clinical signs of acromegaly with typical changes in bone geometry, including increased cortical bone thickness (CBT).
Kristin Godang +8 more
doaj +1 more source
Acromegaly and hypertension [PDF]
Acromegaly is usually caused by pituitary adenomas that secrete growth hormone (GH). The disease is prone to be complicated with hypertension and thus aggravates the state of the illness and increase the disease burden.
WANG Shu-chang, ZHU Hui-juan, PAN Hui
doaj
Aneurysmal dilation of sinus of Valsalva in a patient with undiagnosed acromegaly
Key Clinical Message In patients presenting with aortic ectasia and myxomatous valve diseases at young ages, possible underlying acromegaly should be in mind. Abstract Acromegaly is a chronic systemic disease mainly caused by the benign pituitary adenoma
Hoda Gharoy +4 more
doaj +1 more source
Somatotroph tumors, a rare subtype of pituitary adenomas, can be histologically classified into sparsely granulated (SGSTs) and densely granulated somatotroph tumors (DGSTs) based on cytokeratin staining. SGSTs are generally more invasive and less responsive to medical therapy, making their early identification clinically important.
Le Chen +11 more
wiley +1 more source
Background: Prevalence of hyperprolactinemia in patients with acromegaly is 30 to 40%. Since recently, the necessity of screening for acromegaly in hyperprolactinemic patients with pituitary adenoma has been actively debated. The literature on this issue
Yuliya A. Kukushkina +1 more
doaj +1 more source
Keratinocyte‐Associated Biomarkers Reveal Pathogenic Mechanisms in Acne
The study workflow integrates scRNA‐seq and bulk RNA‐seq data to characterize acne pathogenesis. Step 1 identifies expanded keratinocyte populations using single‐cell analysis. Step 2 filters candidate genes via WGCNA and differential expression integration.
Sini Cai +5 more
wiley +1 more source

