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A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases without surgery.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

A woman developed a hair disorder after a bone marrow transplant, which improved with treatment.

The sebaceous gland plays a significant role in hair loss and thinning, and using growth stimulators, DHT inhibitors, anti-inflammatory drugs, anti-androgens, and super oxide dismuse substances can help manage it.

Scientists created stem cells that can grow hair and skin.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Trichotillomania shows specific signs like black dots and uneven hair lengths but lacks certain features of alopecia areata.

Multiphoton microscopy can non-invasively tell apart scarring from non-scarring hair loss and could aid in treatment.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Inhibiting Zyxin may help treat androgenetic alopecia by promoting hair growth.

An 11-year-old girl's hair loss was caused by a Cladosporium fungal infection, which was cured with itraconazole treatment.

The study found that Short Anagen Syndrome results in short hair growth not due to hair fragility, and hair may grow longer after puberty.

Frequent hairdryer use may worsen hair fragility in people with Pili Annulati.

The "color-transition sign" helps tell apart alopecia areata incognita from telogen effluvium by looking at hair color changes.

Transplanted rat hair follicles grew hair and had increased but not fully restored nerve connections in mice.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

The vitreous membrane in hair follicles changes shape during the hair cycle and may affect hair growth and nutrient exchange.

Alopecia areata is a common autoimmune condition causing varying hair loss, diagnosed by specific patterns of inflammation around hair follicles, with several treatment options available.

Long-term use of minoxidil may cause hair follicles to transform into noticeable terminal hairs, leading to trichostasis spinulosa.

The study found that white hair in vitiligo has specific patterns and structures, which vary with the stage of the disease and may be similar to another hair condition.

Monilethrix is a rare genetic hair disorder that's hard to treat.

The commentary suggests that certain hair and skin care products may be linked to frontal fibrosing alopecia, but not sunscreens, and calls for more thorough research on the causes.

A 38-year-old African American woman has a rare condition that prevents her from growing long hair.

A 4-year-old boy's itchy, scaly scalp and hair loss were correctly diagnosed as tinea capitis after initial misdiagnosis.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Comma hairs are a new sign for identifying scalp fungal infections.