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The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Cidea is essential for proper lipid storage and secretion in sebaceous glands, affecting skin and hair health.

Hair follicle regeneration possible, more research needed.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Many products for hair re-growth exist, but a perfect treatment without side effects has not yet been found.

Adult earlobe can have a benign cyst that is usually removed by surgery.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

The study found that sweat glands contain different types of stem cells that help with healing and maintaining healthy skin.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Some families have a genetic condition where they are born with irregular scalp defects.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Aging causes hair to gray and thin, with the timing of graying varying by race, and factors like oxidative stress and genetics can lead to hair loss.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

The document concludes that while significant progress has been made in understanding skin biology and stem cells, more research is needed to fully understand their interactions with their environment.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Researchers created a fully functional, bioengineered skin system with hair from stem cells that successfully integrated when transplanted into mice.

Melanocyte development from neural crest cells is complex and influenced by many factors, and better understanding could help treat skin disorders.

Assessing newborn scalp hair can reveal important health information.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Melanoblasts migrate to the skin using various pathways, and understanding this process could help with skin disease research.