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Trichotillomania was successfully treated with risperidone and naltrexone.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Fungal infections should be considered in scalp swelling to avoid misdiagnosis.

Trichoscopy helps diagnose frontal fibrosing alopecia in Caucasians, but more research is needed.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Trichoscopy is useful for early detection and monitoring of female pattern hair loss.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

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

Alopecia areata shows a unique type 1 interferon signature, suggesting potential treatment by targeting this pathway.

Men with X-linked recessive ichthyosis can still experience male-pattern baldness.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

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

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

Trichoblastic carcinoma may be a distinct type of skin cancer different from basal cell carcinoma.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

Men with X-linked recessive ichthyosis may not experience typical male-pattern baldness.

Trichoscopy helped diagnose and treat a child's fungal scalp infection by spotting specific hair shapes.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Early detection and removal of hair can prevent damage in hair-thread tourniquet syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Recognizing both trichostasis spinulosa and eruptive vellus hair cysts together is crucial for accurate diagnosis and treatment.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Mutations in specific genes cause different types of ectodermal dysplasias.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

The girl's scalp infection healed well with terbinafine treatment.