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Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Hair follicle bulge cells are important for hair survival and help heal the skin after injury, which might be relevant for understanding hidradenitis suppurativa.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

Alopecia common in teens, may indicate endocrine issue, minoxidil effective treatment.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

People with Telogen Effluvium have similar zinc levels in their blood as healthy individuals.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Two mouse mutants have defective hair cuticle cross-linking.

A boy's hair grew back after he stopped using orthodontic headgear that caused temporary hair loss.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Using patients' own fat-derived cells to treat alopecia areata significantly improved hair growth and was safe.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

Combination therapies work better than single treatments for atrophic acne scars.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Hair disorders need a holistic approach, including medical, cosmetic, and psychological support.

DA-9401 protects against hair loss, improves organ function, and prevents infertility caused by finasteride.

The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

Some common medications can harm male fertility, but many effects can be reversed.

Botulinum toxin shows promise for various skin conditions but requires more research for confirmation and standardized use.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Chemotherapy can cause hair changes similar to alopecia areata, which might lead to misdiagnosis.

Women with female pattern hair loss have higher levels of certain androgens, suggesting increased androgen exposure to hair follicles.