Publications by authors named "Rana Bhattacharjee"

Article Synopsis
  • - Rickets is a condition leading to bony deformities and short stature, which can be caused by a deficiency in calcium (calciopenic) or phosphorus (phosphopenic), making early diagnosis and treatment very important.
  • - A consensus from the Endocrine Society of Bengal aims to simplify the diagnostic approach for rickets, particularly in low-resource settings, and involved extensive discussions, literature review, and agreement by a committee of 29 members.
  • - Key diagnostic steps include examining skeletal deformities, conducting specific blood tests, and utilizing radiographic imaging to confirm rickets, with additional tests recommended for unusual cases or metabolic complications.
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  • * Surgery is the main treatment but often has limited success, leading to tumor recurrence and resistance to standard therapies, necessitating early and diverse treatment strategies.
  • * A case study illustrates successful management of aggressive Cushing's disease using a combination of temozolomide and radiotherapy after surgery failed, alongside etomidate infusion for rapid cortisol reduction.
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Physicians and endocrinologists commonly face various questions related to dietary interventions during clinical encounters with their patients with thyroid disorders. Indeed, both patients and treating physicians have various misconceptions regarding thyroid-specific diets, possibly because of misinformation circulated in lay media or grey literature and the misinterpretation of contradictory scientific data, respectively. In this review, we attempted to answer some frequently asked questions by the patients in the backdrop of contraindicatory perceptions of physicians observed in our survey.

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Introduction: We aimed to describe the clinical, biochemical and etiological profile of patients referred with a provisional diagnosis of rickets in tertiary care centres. In addition, we tried to propose a diagnostic algorithm for the evaluation of such patients.

Methods: This was a retrospective cross-sectional study conducted in two tertiary care centres of West Bengal.

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Background: Gestational diabetes mellitus (GDM) is a prevalent condition with an unclear pathogenesis. B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are potential key players in GDM.

Participants, Materials, And Methods: In a longitudinal observational study, we monitored women from the first trimester through 24-28 weeks of gestation, focusing on the development of GDM.

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Article Synopsis
  • Acute onset of movement disorders, particularly hemichorea-hemiballism, is a recognized but often underreported complication of diabetes, linked to episodes of hyperglycemia.* -
  • A comprehensive literature review from 1950 to October 2023 was conducted, analyzing various case studies and research to understand diabetic striatopathy, including its risk factors and underlying mechanisms.* -
  • Diabetic striatopathy, defined by specific imaging features, is influenced by multiple interconnected factors and may present with symptoms beyond movement disorders, although it generally has a favorable prognosis.*
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Introduction: Considering the inherent vulnerability of immunoassays for heterophilic interference and the potential of Rheumatoid Factor (RF) to act as a heterophile-like antibody, we conducted this study to investigate if RF leads to any such heterophilic interference in seropositive rheumatoid arthritis (RA) patients. The study was done on the TSH assay as it is a noncompetitive, double antibody sandwich assay, which is known to be vulnerable to heterophilic interference.

Methods: In this cross-sectional observational study, eighty-four consecutive newly diagnosed RF-positive RA patients underwent TSH, Free T4, and anti-TPO estimation using the chemiluminescence technique (CLIA) on Siemens Immulite 1000 platform.

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Background: Non-invasive clinic-based tools for assessing PAD are not without limitations. Therefore, costly tests like Doppler study, CT angiography and MR angiography are often required to make a diagnosis. Ankle brachial index (ABI), commonly used for assessment of PAD, has high false positivity rates in sclerosed, calcified arteries which render them non-compressible.

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Purpose: Baseline renal dysfunction predicts mortality in primary hyperparathyroidism (PHPT). However, it remains controversial whether renal insufficiency in PHPT is due to disease severity alone or other risk factors. This study aimed to explore the association of clinico-biochemical variables with renal dysfunction [estimated glomerular filtration rate (eGFR) < 60 ml/min/m] in PHPT.

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Patients with osteomalacia have a low bone mineral density (BMD) and are often misdiagnosed as osteoporosis. A marked increase in BMD is noticed following successful treatment of osteomalacia. The biochemical hallmark of tumour-induced osteomalacia (TIO) is hypophosphatemia.

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Introduction Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder affecting millions of individuals worldwide. Effective management of T2DM is crucial to prevent complications. Dapagliflozin and sitagliptin are oral anti-diabetic agents that have been shown to provide synergistic effects in controlling blood glucose levels.

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  • Hypercalcemia in infants can show various symptoms and its causes change with age; this case involves an infant with nephrocalcinosis and kidney stones.
  • The diagnosis was primary hyperoxaluria (PH) type 2, a rare metabolic disorder, linked with hypercalcemia, which hasn't been documented before.
  • A 9-month-old girl was hospitalized due to a urinary tract infection and was found to have bilateral nephrocalcinosis and a specific genetic mutation, marking a first-ever report of this genetic condition associated with hypercalcemia.
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Objectives: Proximal renal tubular acidosis (pRTA) is characterized by a defect in the ability of the proximal convoluted tubule to reabsorb bicarbonate. The biochemical hallmark of pRTA is hyperchloremic metabolic acidosis with a normal anion gap, accompanied by appropriate acidification of the urine (simultaneous urine pH <5.3).

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  • 46, XX testicular differences of sex development (DSD) is a rare condition where individuals have male phenotypes despite having XX chromosomes, and this case study focuses on an SRY-negative variant.
  • A 3½-year-old child presented with ambiguous genitalia and, after genetic testing, was diagnosed with SRY-negative 46, XX testicular DSD and identified a specific genetic mutation in the NR5A1 gene.
  • This case is significant because it emphasizes the need for further research into underexplored cases of SRY-negative 46, XX testicular DSD, contributing valuable data and insights to the medical community.
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Aromatase (CYP19A1) is the only enzyme known to catalyse the conversion of androgen to estrogen. Aromatase deficiency occurs due to mutation in gene which has an autosomal recessive inheritance pattern. It leads to decrease in estrogen synthesis and delayed epiphyseal closure, eunuchoid habitus and osteopenia.

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  • 46, XY difference/disorder of sex development (DSD) involves varied degrees of underandrogenization in male genitalia, requiring a systematic diagnostic approach due to the lack of standardized clinical guidelines in some regions.
  • A consensus committee of 34 experienced endocrinologists drafted a comprehensive statement addressing diagnostic protocols, emphasizing thorough history taking, clinical examinations, and appropriate hormonal testing.
  • The recommended approach includes formal Karyotyping, tailored biochemical investigations based on age, ultrasound imaging, and utilizing both advanced and accessible hormone measurement techniques.
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  • Hypoparathyroidism is often idiopathic, meaning the causes are usually unknown, but familial idiopathic cases make up a significant portion.
  • The text describes two cases: a middle-aged woman with severe hypocalcemia and a 1-month-old infant experiencing hypocalcemic seizures, both diagnosed with hypoparathyroidism.
  • Genetic analysis identified novel mutations in the GCM2 gene for both patients, highlighting its crucial role in the development and maintenance of the parathyroid gland.
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Many pathologies can cause gonadotropin-independent precocious puberty (GIPP) in prepubertal boys. Leydig cell tumor is one rare cause of this presentation. Here we present a six-year-old boy with features of isosexual precocious puberty, high testosterone levels, low gonadotropin levels, and bone age advancement.

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Purpose Of The Study: Reversible proximal tubular dysfunction associated with distal renal tubular acidosis (dRTA) mimics type 3 RTA, a condition classically associated with features of both proximal RTA (pRTA) and dRTA. Proximal tubulopathy has been reported in children with primary dRTA, but the data in adults are lacking.

Study Design: In this hospital record-based retrospective study, data from 66 consecutive cases of RTA, between January 2016 to December 2018, were retrieved and analyzed.

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