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Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Organs like hair follicles can renew themselves in complex ways, adapting to different needs and environments.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Different combinations of human hair keratins affect how hair fibers form.

A 72-year-old man had severe fatigue, weight loss, and frequent loose stools.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

Scientists identified a group of human skin cells with high growth and regeneration potential.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Nail stem cells and Wnt signaling are important for fingertip regeneration but not sufficient for regenerating more complex limb structures.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

Hair changes can indicate systemic diseases or medication effects.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Lower growth factors linked to balding in androgenetic alopecia.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Disrupted sleep patterns can harm skin and hair cell renewal, but melatonin might help.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Mutation in hairless gene may increase hair loss risk.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

LLLT helps treat hair loss by increasing blood flow, reducing inflammation, and stimulating growth factors.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Hair loss in children is diagnosed and treated differently than in adults, with different common causes and a focus on less invasive methods.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.