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

A 36-year-old woman with low potassium levels was found to have Cushing disease, and after treatment, her potassium levels normalized.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Tralokinumab for atopic dermatitis may cause side effects like dizziness, headache, nausea, hair loss, and acne.

Finasteride may cause changes in dopamine-related genes, possibly leading to post-finasteride syndrome.

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

Cellular senescence may play a role in ALS, and anti-senescence therapies could be a promising treatment.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

The rash resolved after stopping ponatinib.

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

A cat in Turkey had Ehlers-Danlos syndrome, showing very stretchy skin and easy bruising.

Some drugs can cause changes to your hair.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

The method improves hair animation from video by combining image techniques and simulations.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

Trichodynia is a painful scalp condition needing targeted treatments beyond symptom management.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

Psoriasis patients are more likely to experience maladaptive daydreaming.

OnabotulinumtoxinA is used to treat wrinkles, pain, sweating, hair loss, and more by temporarily paralyzing muscles and affecting pain pathways.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Potassium channel modulators mostly increase the activity of rat whisker mechanoreceptors.

Early physiotherapy with exercises and stretching is crucial for treating congenital torticollis.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.