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The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Two siblings have a rare genetic condition causing curly, coarse hair.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

CDP is crucial for lung and hair follicle cell development.

Dermoscopy improves diagnosis of hair and scalp disorders and can help avoid unnecessary biopsies.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Hair loss increases between July and October, possibly due to UV light, and factors like skin type, hair color, and density may affect this. Dandruff can worsen hair loss conditions.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.

The document explains different hair loss types and treatments, emphasizing diagnosis through examination and tests, and specific treatments for each condition.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Testosterone and dihydrotestosterone affect hair growth, and new techniques like the folliculogram help study it, but fully understanding hair growth is still complex.

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.

Androgens can both increase body hair and cause scalp hair loss.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Ginseng and its compounds may help hair growth and prevent hair loss, but more human trials are needed to confirm this.

The document explains hair growth and shedding, factors affecting it, and methods to evaluate hair loss, emphasizing the importance of skin biopsy for diagnosis.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Low iron levels are linked to more hair loss in non-menopausal women.

The girl with autoimmune hair loss might regrow hair within a year, and treatments can help but not prevent recurrence; dermatologist referral and corticosteroids are recommended.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.