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Over half of the students had skin diseases, mainly foot issues and acne, with many unaware or untreated.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Trichostasis spinulosa can look like acne but usually affects adults, not children.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

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

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The boy's symptoms suggest a possible new medical condition.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Hidradenitis suppurativa improves with antiandrogen therapy.

Hair grew in a man's mouth due to a rare condition called heterotopia.

Halo Scalp Ring is a rare newborn hair loss that can be missed, and early diagnosis can avoid extra tests and worry for parents.

Transgender individuals face unique skin issues, often due to hormone therapy, requiring specialized and stigma-free dermatologic care.

Ultrasound can help detect early signs and severity of hidradenitis suppurativa.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Eosinophilic cystitis is often misdiagnosed, but accurate diagnosis and treatment improve outcomes.

Syphilitic alopecia can look like alopecia areata, so careful diagnosis is important.

The baby's hair loss was due to congenital syphilis, which was treated with penicillin.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

SLHA can be hard to diagnose and needs teamwork between specialists.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.