Results 101 to 110 of about 34,733 (291)

CHOLESTASIS, HYPOGLYCEMIA AND UNUSUAL PHENOTYPE AS THE MANIFESTATIONS OF CONGENITAL HYPOPITUITARISM AS PART OF MONOSOMY 18P- SYNDROME

Медицинский совет, 2018
The monosomy 18p-syndrome refers to an extremely rare disorder (1:50,000 live-born infants). Congenital hypopituitarism is one of the manifestations of this syndrome in 13% of cases. The rarity of this pathology causes difficulties in the early detection
A. V. Degtyareva, A. A. Puchkova, A. V. Bolmasova, M. A. Melikyan   +3 more
doaj   +1 more source

Lymphocytic Hypophysitis [PDF]

, 2010
A 59 year-old female presented with visual problems in 2006, and was initially diagnosed with a pituitary macroadenoma on MRI (Figure 1). Preoperatively, the pituitary lesion decreased in size after the patient was started on steroids, raising the ...
Evans, James J., Furlong, Kevin, Kenyon, Lawrence C, Singh MD, Harminder, Singhal, Saurabh   +4 more
core   +2 more sources

Evaluation of the Effect of IL‐1 Antagonists on Pituitary Function

International Journal of Endocrinology, Volume 2026, Issue 1, 2026.
Background Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease frequently observed in populations along the Eastern Mediterranean coast, characterized by recurrent fever, abdominal pain, and joint inflammation. The disease results from mutations in the MEFV gene, which plays a critical role in regulating IL‐1β secretion ...
Fadime Aktas Koc, Baris Sariakcali, Ali Sahin, Vikas Kumar Roy   +3 more
wiley   +1 more source

Characteristics of NAFLD Based on Hypopituitarism

Canadian Journal of Gastroenterology and Hepatology, 2020
Background. Hypopituitarism and hypothalamic disorders, which induce central obesity and appetite disorder, are associated with nonalcoholic fatty liver disease (NAFLD).
Kazuhisa Kodama, Atsuhiro Ichihara, Yasufumi Seki, Yuichi Ikarashi, Takaomi Sagawa, Tomomi Kogiso, Maiko Taniai, Katsutoshi Tokushige   +7 more
doaj   +1 more source

A CASE OF HYPOGLYCEMIA… [PDF]

, 2016
Introdução: O hipopituitarismo é caracterizado por insuficiência da secreção hormonal hipófisária. A clínica é variável e depende da etiologia, evolução temporal e hormonas envolvi- das.
Afonso, Ariana, Antunes, Ana, Gomes, Maria Miguel, Marques, Olinda, Martins, Sofia, Pereira, Ângela, Silva, Helena   +6 more
core  

Penile length and anogenital distance in male newborns from different Iranian ethnicities in Golestan Province [PDF]

, 2014
Background: Anogenital distance (AGD) is a feasible and accepted parameter of exogenous or endogenous androgens effects on development of reproductive ...
Alaee, E., Fouladinejad, M., Gharib, M.J.   +2 more
core   +1 more source

Precision Diagnostics in Sports‐Related Traumatic Brain Injury: Pathophysiology, Biomarker Development and Emerging Technologies

Advanced Sensor Research, Volume 4, Issue 12, December 2025.
Sports‐related traumatic brain injuries (TBIs) remain underdiagnosed, within amateur athletic cohorts. This review critically synthesises recent advancements in AI‐assisted neuroimaging, blood‐based biomarker profiling, wearable biosensing platforms for early detection, injury stratification, and longitudinal surveillance of TBIs.
Daniel Nicol, Mohamed T. Patel, Debarati Bhowmik, Pola Goldberg Oppenheimer   +3 more
wiley   +1 more source

Pituitary dysfunction following traumatic brain injury: clinical perspectives

Neuropsychiatric Disease and Treatment, 2015
Fatih Tanriverdi, Fahrettin Kelestimur Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey Abstract: Traumatic brain injury (TBI) is a well recognized public health problem worldwide.
Tanriverdi F, Kelestimur F
doaj  

Hypopituitarism after subarachnoid haemorrhage, do we know enough? [PDF]

, 2014
BACKGROUND: Fatigue, slowness, apathy and decrease in level of activity are common long-term complaints after a subarachnoid haemorrhage (SAH). They resemble the symptoms frequently found in patients with endocrine dysfunction.
Diederik WJ Dippel, Fop van Kooten, Gerard M Ribbers, Karin Blijdorp, Ladbon Khajeh, Sebastian JCMM Neggers   +5 more
core   +4 more sources

Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis.

Journal of Clinical Endocrinology and Metabolism, 2018
CONTEXT Congenital hypopituitarism (CH) is rarely observed in combination with severe joint contractures (arthrogryposis). Schaaf-Yang syndrome (SHFYNG) phenotypically overlaps with Prader-Willi syndrome, with patients also manifesting arthrogryposis. L1
L. Gregory, P. Shah, J. Sanner, M. Arancibia, J. Hurst, W. Jones, H. Spoudeas, Polona Le Quesne Stabej, H. Williams, L. Ocaka, C. Loureiro, A. Martínez-Aguayo, M. Dattani   +12 more
semanticscholar   +1 more source