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2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

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

The laser system helps study brain cell functions by precisely removing specific cells and observing changes.

A child with a rare scalp condition regrew hair after treatment.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

ADEM is a sudden brain disorder often following infection or vaccination, diagnosed by ruling out other conditions.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

Hamilton scale imprecise, hair shaft diameter decreases, stem cell transplant regrows hair, ECP ineffective for alopecia areata universalis.

A special diet can fix hair problems in argininosuccinase deficiency.

Intralesional steroids effectively treated a young female's scalp nodules without recurrence.

ACOD1 deficiency worsens hair loss by causing cell aging and mitochondrial problems, but 4-OI may help.

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

Cicatricial alopecia can progress to complete hair loss, making diagnosis and management difficult.

Accurate diagnosis is crucial for effectively treating severe alopecia and related symptoms.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A 32-year-old woman's hair loss was linked to skin nodules and severe headaches.

Other common signs, not just the well-known immune cells around hair bulbs, are important for diagnosing hair loss from alopecia areata.

A new type of sudden, complete female hair loss was found, with most patients fully recovering within 6 months without needing steroid treatment.

Hair thickness differences help diagnose hair loss severity.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The woman's hair loss might be due to a chronic infection.

The woman has a skin condition involving nodules, scars, and hair loss.

Frontal fibrosing alopecia is linked to increased immune system activity and reduced stem cells, suggesting early treatment targeting this pathway might prevent hair follicle damage.