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The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

The document concludes that more research is needed to fully understand the causes of PCOS.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The SARS-CoV-2 vaccine may be linked to triggering autoimmune conditions like Alopecia Areata.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

The article suggests that patients with Frontal Fibrosing Alopecia may have more contact allergies, but it doesn't prove that allergies cause the condition.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

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

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Alopecia Areata is a hair loss condition affecting all genders, often linked to other diseases, with treatments available but varying success rates.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

FFA's causes may include environmental triggers and genetic factors.

The document concludes that early recognition and treatment of primary cicatricial alopecia is crucial to prevent permanent hair loss.

The conclusion is that acne, alopecia, and hyperhidrosis are common skin issues with various treatments available, and accurate diagnosis is key for effective management.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

Gene linked to common hair loss found, may lead to new treatments.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Trichotillomania, a disorder where people compulsively pull out their own hair, often starts around age 12, is more common in adult females, and can be treated with behavior therapy and medication.

AGA treatments like minoxidil and LLLLT are safe and effective for gender minority patients.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Lichen planopilaris is the most common type of scarring hair loss observed, with a variety of symptoms and tissue changes.