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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Ultrasound shows 80% of Hidradenitis Suppurativa patients have abnormal hair tracts that may worsen the condition.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Hair follicle stem cells could be used to treat the skin condition vitiligo.

Elkonyxis, a rare nail condition, improved when patients stopped their nail-picking habits.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Dandruff might be caused by changes in how hair follicles naturally release oils and an immune response to this imbalance.

Two young cats with a severe ear and skin condition improved with immune system-targeting treatments.

A woman's hair loss looked like a different condition due to her hairstyle, and treatment stopped further hair loss but didn't regrow hair.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document concludes that Loose Anagen Hair Syndrome is a benign condition where hair is thin and easily pulled out, often improving with age.

A woman's hair loss was initially mistaken for a common hair loss condition but was later found to be caused by breast cancer cells in her scalp.

Two patients with skin lupus were mistakenly thought to have a different scalp condition but improved with lupus treatment.

Psoriasis lesions have fewer and smaller oil glands, which might affect the condition's development.

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

A rare benign skin nodule was found on the buttock, a unique location for this condition.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

IL-33 is linked to hair follicle damage in psoriasis and could be a treatment target for hair loss in this condition.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Researchers improved a method to study individual cells in newborn mouse skin and found a way to assess the severity of a skin condition in humans.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.