Publications by authors named "Partha Chakraborty"

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.
View Article and Find Full Text PDF
Article Synopsis
  • * 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.
View Article and Find Full Text PDF

Objective: Thyroid diseases pose a substantial socioeconomic burden globally. The aim of this study was to evaluate the correlation between estradiol-to-testosterone (E2/T) ratio and thyroid peroxidase antibody (TPOAb) positivity in male patients with hypothyroidism or euthyroidism.

Subjects And Methods: Cross-sectional observational study including 115 male patients with hypothyroidism or euthyroidism.

View Article and Find Full Text PDF

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.

View Article and Find Full Text PDF

Morbidity and mortality rates in patients with autosomal recessive, congenital generalized lipodystrophy type 4 (CGL4), an ultra-rare disorder, remain unclear. We report on 30 females and 16 males from 10 countries with biallelic null variants in CAVIN1 gene (mean age, 12 years; range, 2 months to 41 years). Hypertriglyceridemia was seen in 79% (34/43), hepatic steatosis in 82% (27/33) but diabetes mellitus in only 21% (8/44).

View Article and Find Full Text PDF

Drying front propagation and coupled heat and mass transfer analysis from porous media is critical for soil-water dynamics, electronics cooling, and evaporative drying. In this study, de-ionized water was evaporated from three 3D printed porous structures (with 0.41 mm, 0.

View Article and Find Full Text PDF

Introduction: A structured dedicated health programme for Type 1 diabetes mellitus (T1DM) has been initiated in the state of West Bengal, India.

Aim: The aim is to provide comprehensive healthcare to all children, adolescents and young adults living with T1DM, along with the provision of free supply of insulin, glucose measuring devices, blood glucose test strips, and other logistics. The strategic framework for programme implementation is to utilise the infrastructure and manpower of the already existing non-communicable disease (NCD) clinic under National Health Mission.

View Article and Find Full Text PDF

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.

View Article and Find Full Text PDF

Whether and how the spatial arrangement of a population influences adaptive evolution has puzzled evolutionary biologists. Theoretical models make conflicting predictions about the probability that a beneficial mutation will become fixed in a population for certain topologies like stars, in which "leaf" populations are connected through a central "hub." To date, these predictions have not been evaluated under realistic experimental conditions.

View Article and Find Full Text PDF

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).

View Article and Find Full Text PDF

Functional abdominal pain disorders (FAPDs) affect up to 25% of children in the United States. These disorders are more recently known as disorders of "brain-gut" interaction. The diagnosis is based on the ROME IV criteria, and requires the absence of an organic condition to explain the symptoms.

View Article and Find Full Text PDF

Background: One of the common causes of suboptimal control of thyroid stimulating hormone (TSH) in levothyroxine-treated hypothyroidism is coadministration of proton pump inhibitors (PPIs). Morning administration of pantoprazole has been shown to suppress intragastric pH to a greater extent. We therefore aimed to determine the effect of pantoprazole at different time points of the day on thyroid function test (TFT) in levothyroxine-treated overt primary hypothyroidism.

View Article and Find Full Text PDF

Background: An additional flap during the tubularization of incised urethral plate urethroplasty (TIPU) is believed to minimize the postoperative complications. It is still debatable whether using an additional flap is worth the risk given the hazards associated with doing so. This study aims to re-evaluate the benefits and drawbacks of TIPU with or without a preputial dartos (PD) flap.

View Article and Find Full Text PDF
Article Synopsis
  • 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.
View Article and Find Full Text PDF

Background: A survey of neonates with esophageal atresia and tracheoesophageal fistula (EA ± TEF) to determine additional factors responsible for poor surgical outcomes in our institution where employing an improved standard of care can ameliorate the outcome.

Materials And Methods: We carried out a retrospective review of 54 neonates, who underwent surgical repair of EA± TEF over a 5-year period. We collected data regarding the patients' demographics, perioperative findings, records of neonatal intensive care, and ascertained the effects of gender, gestational age, birth weight, age at operation, type of anomaly, coexisting major anomalies, preoperative inotrope therapy, and duration of postoperative ventilation on the surgical outcome.

View Article and Find Full Text PDF

Enamel renal syndrome (ERS) due to loss of function (LOF) mutation of FAM20A gene typically consists of hypoplastic amelogenesis imperfecta (AI) and bilateral nephrolithiasis/nephrocalcinosis. Recent evidence suggests that FAM20A interacts with FAM20C and increases its activity; thus LOF mutation of FAM20A leads to impaired FAM20C action. FAM20C, a golgi casein kinase, phosphorylates fibroblast growth factor (FGF)-23, prevents its glycosylation and makes it more susceptible to degradation by furine proteases.

View Article and Find Full Text PDF

Objective: Thyroid dermopathy (TD), reportedly encountered in less than 5% of patients with Graves' disease (GD), is supposed to coexist only with thyroid-associated orbitopathy (TAO). However, clinically inapparent TD, detected non-invasively by thermal imaging or ultrasonography, seems to be present in a larger proportion of GD. Histopathological examination (HPE), though considered as gold standard for detecting TD, has not been performed widely to identify subclinical TD in GD.

View Article and Find Full Text PDF

This study assessed physician and parent perceptions regarding plant-based beverage consumption in children. We surveyed 128 physicians and 215 parents of patients at University of Miami and Jackson Memorial Hospital. Among physicians, 52% recommended plant-based beverages, typically soy (33%), for cow's milk allergy (32%).

View Article and Find Full Text PDF

Adults with distal renal tubular acidosis (dRTA) commonly present with hypokalaemia (with/without paralysis), nephrolithiasis/nephrocalcinosis and vague musculoskeletal symptoms. All adults with dRTA should be thoroughly evaluated for systemic diseases, certain medications and toxins. The leading cause of acquired or secondary dRTA in adults is primary Sjögren syndrome (SS); however, other collagen vascular diseases (CVDs) including seronegative spondyloarthropathy (SSpA) may at times give rise to secondary dRTA.

View Article and Find Full Text PDF

At present, a multifaceted clinical disease known as heart failure disease can affect a greater number of people in the world. In the early stages, to evaluate and diagnose the disease of heart failure, cardiac centers and hospitals are heavily based on ECG. The ECG can be considered as a regular tool.

View Article and Find Full Text PDF

Dipsogenic polydipsia (DP), a distinct variety of primary polydipsia, is characterised by selective diminution of osmotic threshold for thirst leading to polydipsia and subsequent hypotonic polyuria. Seen in patients without underlying psychiatric illness, DP closely mimics central diabetes insipidus (CDI), making it difficult for clinicians to discriminate these two conditions from each other. Carefully performed osmotic stimulation study, incorporating objective assessment of threshold for thirst and arginine vasopressin (AVP) release is the key to differentiate DP from CDI or psychogenic polydipsia, also termed compulsive water drinking (CWD).

View Article and Find Full Text PDF