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Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

People with certain skin diseases often have more trouble understanding and describing their emotions, which can affect their health and treatment results.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Women with PCOS in Sicily show different levels of metabolic problems depending on their PCOS type, with obesity and abnormal lipid profiles being common.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Using baked goods as visual aids helps people understand skin conditions better.

Following a specific clinical sequence can help diagnose and treat Demodex mites in the eyes.

Sandalore®, a synthetic scent, reduced hair loss and improved hair growth in women with telogen effluvium.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Olive oil helps Malassezia globosa overgrow, worsening atopic dermatitis in mice.

Microstimulation of certain facial and mouth nerves can evoke specific sensations, while deeper nerves may require multiple stimulations to affect perception.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

The twins' condition is unique and doesn't match any known syndromes.

Dystonia may be part of PAS-4 and linked to immune issues.

Married Egyptian women with PCOS have lower sexual desire compared to those without PCOS.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

COVID-19 may cause temporary hair loss due to direct damage to hair follicles, but it usually gets better on its own.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Ascorbic acid, orlistat, and mastic gum can effectively reduce sweat odor.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Madarosis (eyebrow and eyelash loss) significantly affects quality of life for breast cancer patients on taxane-based chemotherapy.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Recurrent dry cough, wheezing, and respiratory discomfort are key symptoms for diagnosing pediatric asthma.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Early recognition and multidisciplinary management are crucial for improving outcomes in Parry-Romberg syndrome.

Blocking CISD1 reduces hearing loss from cisplatin in mice.