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A runner developed tangled armpit hairs from shirt friction, preventable by shaving or wearing smooth shirts.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

A 14-year-old boy was diagnosed with a rare hair condition that may lead to hair thinning and has no known effective treatments.

Monilethrix causes brittle hair and hair loss, and it runs in families.

Treatment improved some symptoms but not all.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

The article simplifies trichoscopy terms and offers a new diagnostic flowchart.

A Chinese boy's scalp infection from a guinea pig was cured with medication.

Ciclosporin can cause excessive hair growth even with testosterone blockers.

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

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

Lichen planopilaris can occur with multiple autoimmune diseases.

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

A female Rottweiler had a rare genetic condition causing mostly hairless skin.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Trichotillomania is a hair-pulling disorder needing different treatments than OCD.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Corticosteroid injections for hair loss may cause eye problems, so caution is needed.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Early detection and treatment of hair-thread tourniquet syndrome in young girls is important to prevent serious harm.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Targeting the endocannabinoid system might help reduce hair pulling in trichotillomania.

Tigason improved hair growth in a boy with monilethrix without side effects.