Congenital adrenal hyperplasia (CAH) constitutes a group of genetic disorders primarily originating from mutations in the CYP21A2 gene, responsible for encoding the adrenal steroid 21-hydroxylase enzyme (P450c21). This genetic anomaly results in impaired adrenal steroidogenesis and is inherited as an autosomal recessive trait.
Pituitary adenomas represent a common subset of sellar region tumors, typically presenting with a diverse array of clinical manifestations. Among the myriad challenges these adenomas pose, calcification is rare and often raises suspicion of alternate diagnoses, such as craniopharyngiomas.
Osteomyelitis, primarily caused by Staphylococcus aureus infection, is a prevalent condition. While over 100,000 fungal species are described, only 150 are pathogenic to humans. Opportunistic infections, often when host defenses are compromised or through invasive gateways like dental extractions or traumatic skin discontinuities, pose challenges in timely diagnosis and treatment.
In a significant stride towards combating the pervasive impact of cancer, the Department of Health (DOH) and the World Health Organization (WHO) have jointly unveiled the 2024-2028 National Integrated Cancer Control Program (NICCP) Strategic Framework.
Parkinson’s disease has been a formidable challenge for medical professionals worldwide. It is a neurodegenerative disorder that is challenging to manage effectively due to its complex interplay of genetic predisposition, environmental factors, and a wide range of symptoms.
Head and neck cancers (HNCs) represent a significant global health burden, with oral cancer being particularly prevalent in regions like India. In response to this challenge, the Oral Cancer Task Force (OCTF), supported by the Biocon Foundation, has developed consensus guidelines for managing head and neck cancer.
We present a case involving a young East Asian child diagnosed with multisystem inflammatory syndrome in children (MIS-C). The toddler had a two-day fever accompanied by pyuria and, five weeks prior, had recovered from COVID-19.
A groundbreaking study at King’s College London has delved into the intricate world of infant brain development, revealing distinct patterns in moment-to-moment activity and connectivity between Preterm and term infants.
Diabetes mellitus (DM) has long been a silent menace characterized by elevated blood glucose levels and metabolic imbalances.
In recent years, medical technology has made significant strides, ushering in innovative and less invasive treatments that have transformed the surgery landscape.
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