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Hair loss severity relates to increased miniaturization in female pattern hair loss.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Hair follicles are hormone-sensitive and involved in growth and other functions, with potential for new treatments, but more research is needed.

An mFG score of 5 or more indicates above-normal hair growth in Southern Chinese women.

There are many treatments for permanent hair loss disorders, but their effectiveness varies and there's no clear best option.

Many people had severe allergic reactions to a common hair dye ingredient, causing them to seek medical care and miss work.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The document concludes that accurate diagnosis and personalized treatment are important for skin problems in women with PCOS.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Pregnancy can cause skin pigmentation, stretch marks, and changes in hair, nails, and sweat glands, with most resolving after birth.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Alopecia areata treatment varies, with no optimal method established yet.

Treatments for permanent hair loss from scarring aim to stop further loss, not regrow hair, and vary by condition, with partial success common.

Male pattern baldness involves smaller hair follicles, larger oil glands, and other tissue changes, but not major blood supply issues.

Improving skin barrier and using antifungal treatments can help manage dandruff.

Finasteride improves hair loss in women with hyperandrogenism.

Polygonum multiflorum extract helps grow hair by activating certain hair growth signals in mice.

The document concludes that molluscum contagiosum is a common, benign skin infection in children, often healing without scarring.

Lichen planopilaris is a chronic, scarring hair loss condition with no definitive cure, requiring accurate diagnosis and treatment to manage symptoms.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

Growth factors are crucial for hair development and could help treat hair diseases.

Trichoscopy helps diagnose and monitor alopecia areata by looking at a combination of specific hair and scalp features.

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

Fetal skin heals without scarring due to unique cells and processes not present in adult skin healing.

New antifungal treatments for a children's scalp infection are effective and safe, but it's not decided if they will become the preferred option over the old treatment.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Type 2 diabetes, bacterial scalp infections, and tight hairstyles like braids and weaves are linked to a higher risk of a scarring hair loss condition in African American women.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

Vitiligo is linked to autoimmune diseases and hearing issues, so hearing tests are recommended for patients.