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This research reports a new autosomal recessive mutation in mice, 'lanceolate hair', causing generalized alopecia and hair shaft abnormalities, which may serve as a model for Netherton's syndrome in humans.

This study identified a new mouse mutation associated with noninflammatory proliferative skin disease and hair abnormalities, drawing parallels to human conditions like Netherton's syndrome and monilethrix.

This observational retrospective study conducted at Lahore General Hospital reported that scabies, followed by tinea and acne, were the most common skin diseases, primarily affecting females and prevalent in the summer months among the studied population.

This study observed that among Doctor of Physiotherapy students in Lahore, the prevalence of androgenetic alopecia was 55.6% in males and 60% in females, highlighting the need for better public education and early treatment strategies.

This study found a weak association between Cyp11a1 gene variation and polycystic ovary syndrome, with higher di-hydro-testosterone levels observed in individuals with the syndrome and anovulatory PCOS compared to controls.