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RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A rabbit gene important for hair development was identified and detailed.

A 6-year-old girl with head lice developed scarring hair loss but improved with treatment.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

The Sacred Heart Bilobed Flap is a surgical method for repairing small scalp defects with local flaps, relying on scalp elasticity and hair regrowth to hide any imperfections.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

The document outlines steps for moving fat from one body part to another.

The herbal lip hydrant is more effective than petroleum gel for improving lip hydration and reducing chapped lips.

Wearing a wig caused a woman's skin condition to worsen due to pressure from the wig's fasteners.

A new mutation in mice causes crooked whiskers and messy hair.

Wearing a wig caused a skin condition to develop in a woman with hair loss.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

A rare gene variant causes hair and nail issues in a family.

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

The four patients have a unique type of ichthyosis affecting hair follicles.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Scalp edema may be a new variant of conditions reacting to scarring alopecia like LPP.

Bird foot scales develop differently and can repair but not fully regenerate due to the lack of specialized stem cell areas.

The laser treatment effectively and safely improved keratosis pilaris.

Keratin-associated proteins are part of the developing hair fiber cuticle.

Treat active lichen planopilaris early to prevent permanent hair loss.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

Mixing platelet-rich plasma with Poly-D,L-Lactic Acid helps reduce deep lines around the nose and mouth.