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The study found that Temporal Triangular Alopecia often starts in early childhood, mainly affects the left side of the scalp, and has no effective treatment except surgery.

Oral minoxidil effectively increases hair growth in male baldness but can cause side effects like excessive hair growth and swelling.

Oral minoxidil improved male baldness, but had side effects; certain antibiotics effectively treated a rare scalp condition; hair transplants might trigger another scalp condition.

Keratin hydrogels from human hair show promise for tissue engineering and regenerative medicine.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

The document concludes that treating skin conditions should include psychological care and a multidisciplinary approach is essential for effective management.

Smoking and drinking can lower vitamin levels and potentially trigger early hair loss, but overall vitamin levels don't seem to affect hair loss duration.

Hair loss in women, often not related to male hormones, increases with age and can cause significant emotional distress.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

The study found nine new hair protein genes in human hair follicles.

The conclusion is that treatments for Telogen Effluvium exist, but standard treatment guidelines are needed.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Holes in mature hair are likely caused by the removal of substances during hair care.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

People with TED often have low B12 levels and might benefit from B12 supplements.

Telomerase-positive cells are mainly in the bulb matrix and outer root sheath of hair follicles.

The study found that Frontal Fibrosing Alopecia in North-East India mainly affects middle-aged women and is often associated with lichen planus pigmentosus.

Human hair keratin can be used in many medical applications.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Hair curvature in Japanese people is linked to specific cell types and filament arrangements in the hair cortex.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Protein composition greatly affects the function of keratin biomaterials.

Cyclosporin A promotes hair cell growth and affects protein kinase C levels.

Low-dose naltrexone helps reduce symptoms and slow down lichen planopilaris without side effects.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.