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A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Early diagnosis and comprehensive treatment can significantly improve trichotillomania in children.

Manatee whiskers are specially adapted for touch in water.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Copper therapy improved health and enzyme activity in mice with copper deficiency.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

HLD10 can include increased body hair and Mongolian spots.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Multiple pilomatrixoma may indicate Turner syndrome.

Minoxidil sulfate relaxes muscle by increasing potassium flow, making it a unique muscle relaxer.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

The patient showed signs of liver disease due to alcohol use but didn't need treatment for Dupuytren’s contracture.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

Blocking GABA(A) receptors increases neuron sensitivity, showing GABA and glycine have different roles in pain.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

A girl with Pitt-Hopkins syndrome developed curly hair as a rare side effect from the epilepsy drug perampanel.

Hypertrichosis causes excessive hair growth and needs psychological support due to its impact on self-esteem.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

Animal hair can curl tightly on its own, especially in foxes, due to changes in keratin.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

Effective treatments for trichotillomania include cognitive-behavioral therapy, certain medications, and alternative support tools.

Nephronectin helps attach muscle cells to hair follicles.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.