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Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Women with telogen effluvium have lower levels of iron, folate, and vitamin B12.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Epithelial stem cells are crucial for tissue renewal and repair, and understanding them could improve treatments for damage and cancer.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

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

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

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

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Changing Wnt signaling can lead to more or less hair growth and might help treat hair loss and skin conditions.

Tiny particles called extracellular vesicles could help with skin healing and hair growth, but more research is needed.

New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

Some families have a genetic condition where they are born with irregular scalp defects.

Scientists have made progress in creating replacement teeth, hair, and glands that work, which could lead to new treatments for missing teeth, baldness, and dryness conditions.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.