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Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Hair follicle stem cells need all reprogramming factors to become pluripotent.

New treatments for hair growth disorders are needed due to limited current options and complex hair follicle biology.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

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

Eating a balanced diet with the right vitamins and minerals is important for healthy hair, but too many supplements can be harmful.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Silk proteins are great for cosmetics because they protect and improve skin and hair while being eco-friendly.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

The environment around melanocyte stem cells is key for hair regeneration and color, with certain injuries affecting hair color and potential treatments for pigmentation disorders.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

LED light therapy is effective for skin and hair treatments but requires careful use to minimize risks.

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

The document concludes that Loose Anagen Hair Syndrome is a benign condition where hair is thin and easily pulled out, often improving with age.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

The Bcl-2 protein is important for keeping hair follicle stem cells working and preventing hair loss.

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.

CD2 might be a new treatment target for patchy alopecia areata.

Stem cells are crucial for skin repair and new treatments for chronic wounds.

Different types of stem cells with unique roles exist in blood, skin, and intestines, and this variety is important for tissue repair.

SDF-1/CXCL12 and its receptor CXCR4 are crucial for melanocyte movement in mouse hair follicles.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The balance of thiol-disulfide in women with hair loss is affected but not damaged.