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Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Acute illnesses like sepsis can disrupt thyroid hormone balance without central hypothyroidism.

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

A horse with severe hair loss was diagnosed with alopecia areata and a yeast infection.

Mitochondrial stress can lead to atopic dermatitis.

Hair loss and polyneuropathy improved, but severe vision impairment persisted.

Low zinc and selenium levels in sheep are linked to hair loss and thyroid problems.

The ZIP13 variant is linked to abnormal hair quality.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Most patients with autoimmune blistering diseases experienced some hair loss, which may be underreported and linked to disease severity.

Hair medullary cells in mammals vary in complexity, with humans having more structured cells similar to inner root sheath cells.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Follicular structures help differentiate keratoacanthoma from squamous cell carcinoma.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Loss of keratin K2 causes skin problems and inflammation.

A girl's severely tangled hair couldn't be fixed and had to be cut due to a rare condition called plica neuropathica.

Scalp lesions in discoid lupus are more common in women and linked to other autoimmune diseases.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Trichoscopy helped diagnose a teenage girl's hair loss as monilethrix.

Different diseases cause specific skin and hair follicle changes in dogs with alopecia.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Clinicians should recognize taste disorders and hair loss as important symptoms in myasthenia gravis patients.

The Gsdma3 gene is essential for normal hair development in mice.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.