16 results match your criteria: "Aadhar Health Institute[Affiliation]"

Unlabelled: Pheochromocytoma and paraganglioma (PPGL) have been associated with low bone mineral density (BMD) due to excess sympathetic system stimulation. Our study revealed low BMD and TBS (trabecular bone score) in cases compared to matched controls. Plasma-free nor-metanephrine and hypertension duration found to be most consistent predictive factors.

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Russell-Silver syndrome (RSS) is a rare genetic disorder characterized by intrauterine growth restriction (IUGR), postnatal growth failure, and distinctive dysmorphic features. We present a case of a four-year-old male presenting with a slow growth velocity with a history of IUGR and surgical interventions, exhibiting classic RSS features. Laboratory investigations revealed low insulin-like growth factor 1 (IGF-1) and low growth hormone (GH) levels on stimulation tests.

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Article Synopsis
  • The study aimed to assess whether elevated fasting plasma glucose (FPG) levels in the first trimester can predict the development of gestational diabetes mellitus (GDM) later in pregnancy, as well as associated adverse events.
  • It analyzed data from 16 studies involving over 115,000 pregnancies and found that FPG levels above 5.1 mmol/L (92 mg/dL) significantly increased the risk of GDM and several pregnancy complications including pre-eclampsia and large-for-gestational-age infants.
  • However, the research had limitations, such as a lack of diverse studies reporting on higher FPG thresholds, particularly at 6.1 mmol/L (110 mg/dL).
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Erratum to Correct Informed Patient Consent Statement.

touchREV Endocrinol

April 2024

Department of Gastroenterology, Aadhar Health Institute, Hisar, Haryana, India.

Article Synopsis
  • It addresses an update or correction related to the original article with the DOI 10.17925/EE.2023.19.2.6.
  • The correction aims to clarify important data or conclusions presented in the original research.
  • This ensures that readers have accurate and reliable information for reference in their studies.
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Background: Pheochromocytoma, the great masquerader, can have a varied spectrum of clinical manifestations. It can often cause a diagnostic challenge despite the availability of modern investigation modalities.

Case: We present the case of a 38-year-old male who presented with uncontrolled hypertension for the past 10 years and heart failure for one year.

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Background: Endocrinology has been a popular choice of super-specialisation in India in recent years. The PURsuit of Endocrinology (PURE) survey aims to determine the factors that facilitated the selection of endocrinology as the area of super-specialisation among first-year residents across India.

Methods: We conducted an electronic questionnaire-based survey among first-year residents across India.

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Parathyroid carcinoma is a rare endocrine neoplasm that accounts for <1% of cases of primary hyperparathyroidism. The management of parathyroid carcinoma is a challenge due to the high rate of local recurrence of the tumour. We report the case of a middle-aged north Indian woman who presented with recurrent primary hyperparathyroidism due to parathyroid carcinoma.

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Introduction: Early detection and diagnosis of diabetic autonomic neuropathy, especially cardiac autonomic neuropathy (CAN), have gained attention recently because of their elevated cardiovascular mortality risk. Although the connection between type 2 diabetes mellitus and autonomic neuropathy is well established, evidence is emerging that the association might predate the stage of prediabetes.

Objective: The present study was undertaken to compare the prevalence of CAN in prediabetes versus that in normoglycemic controls.

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Article Synopsis
  • Monogenic obesity can be caused by mutations in single genes related to hunger and satiety, with the leptin receptor (LEPR) gene mutation being one of the rare causes leading to early-onset obesity and other metabolic issues.
  • A case study of a 12-month-old boy showed rapid weight gain and hyperphagia, with genetic tests revealing a novel, damaging variant in the LEPR gene that was categorized as a variant of uncertain significance.
  • The family sought financial assistance for treatment with setmelanotide, a new therapy for monogenic obesity linked to LEPR mutations, indicating a gap between healthcare needs and resources for affected families.
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Epigenetics of type 2 diabetes mellitus (T2DM) has widened our knowledge of various aspects of the disease. The aim of this review is to summarize the important epigenetic changes implicated in the disease risks, pathogenesis, complications and the evolution of therapeutics in our current understanding of T2DM. Studies published in the past 15 years, from 2007 to 2022, from three primary platforms namely PubMed, Google Scholar and Science Direct were included.

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The development of standardized reporting systems is of paramount importance in medical-imaging. Based on the "RADS" methodology, PIRADS and BI-RADS have been successfully used. The management of bladder cancer (BC) depends on the stage at the time of identification.

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Diabetes mellitus can be associated with a variety of musculoskeletal disorders. Diabetic cheiroarthropathy or diabetic hand syndrome is one of the complications encountered in long-standing uncontrolled diabetes. It is characterized by limited movement of the joints of the hands along with thickening of the skin on the palmar and dorsal surfaces.

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Objective: To evaluate the bioequivalence of a hybrid pegylated liposomal doxorubicin (PLD) hydrochloride injection with reference product Caelyx®.

Methods: This multicenter, open-label, balanced, randomized, two-treatment, two-period, two-sequence, single-dose, crossover, bioequivalence study was conducted in female patients aged ≥18 years and ≤75 years with ovarian cancer, whose disease progressed or recurred after platinum-based chemotherapy, and who were scheduled to start PLD therapy. Patients were intravenously infused drugs over 1 h at 50 mg/m dose two hours after breakfast on the first day of the chemotherapy cycle in period-I and crossed over to the other arm in period-II (day 29).

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