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Higher DHT levels are linked to worse heart changes in severe aortic valve stenosis patients.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Young patients with Vogt-Koyanagi-Harada syndrome may have poor vision outcomes despite treatment due to frequent recurrences.

Young women with PCOS without additional risk factors may have normal heart function.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A new teledermatology system improved access and reduced wait times for skin care.

Intralesional cidofovir might be a good alternative treatment.

Vascular Surgery should become an independent discipline with its own board for a better future.

Early diagnosis and aggressive treatment are essential for managing Vogt-Koyanagi-Harada syndrome effectively.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Recognizing CVG can help diagnose systemic amyloidosis early.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

MSF-VMDNet accurately segments skin cancer images better than existing methods.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

The regenerative solution, tSVF, is a safe and effective treatment for various conditions like aged skin, scars, wounds, and more, but more research is needed to find the best way to use it.

Psoriasis can cause rare vulval scarring.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

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

A Cavalier King Charles Spaniel had both uveodermatological syndrome and alopecia areata, and treatment with ciclosporin helped regrow hair.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.