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Hidradenitis suppurativa treatment should be tailored to the individual, with quitting smoking being important.

Cats with atopic dermatitis often have severe, year-round itching and respond well to certain treatments.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Men with enlarged prostates often have more severe baldness.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

Artificially inducing hair regrowth in mice can change the normal pattern and timing of hair growth, with minimal color differences between old and new fur.

Cosmetics enhance beauty, fix defects, and intimidate enemies, with varying cultural standards and alternative methods.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Men with early hair loss have similar hormone levels to women with PCOS, possibly increasing risk of obesity and heart issues.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

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

Adrenal disorders can cause lasting brain and behavior issues in children.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Early diagnosis and treatment of TPP can prevent complications.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Hedychium spicatum has medicinal properties but needs more research for scientific validation and use.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Oral zinc sulphate reduces dark hair color in mice.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.