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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Trichoscopic features help diagnose and assess female pattern hair loss severity, with inflammation playing a key role.

A fungal infection developed on a herpes scar and was successfully treated with antifungal medication.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A woman's eyelashes grew thicker and longer after taking topiramate, but returned to normal when she stopped the medication.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

Taste disorders in Cronkhite-Canada syndrome are severe in the front of the tongue but improve with treatment.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Her hair grew back normally after she stopped rubbing it.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Chronic scalp pain in trichodynia involves both body-wide and localized increased pain sensitivity.

Better-designed, long-term studies are needed to optimize treatment for trichotillomania and trichophagia.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Hair shaft disorders often indicate genetic or systemic issues and are managed by minimizing damage.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Kerion is a rare but serious scalp infection that needs proper treatment.

Hair-thread tourniquet syndrome needs more awareness and discussion in dermatology.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

The girl has an inflammatory type of scarring hair loss.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A new DSG4 gene mutation causes hair defects in a young girl.

Diagnosing and managing children's hair shaft disorders is challenging but essential.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.