Search

everythinglearnresearchcommunity

for

Search:↓

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Unani medicine may help treat a rare, hard-to-treat hair loss pattern in children.

The belief about hair shedding phases is likely incorrect and needs reevaluation.

Keratinized wool cells still have some organelles like lysosomes and mitochondria.

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Focal atrichia helps diagnose female pattern hair loss.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

The cream effectively reduced hair growth on forearms.

Oxidative stress and mitophagy play key roles in hair loss, suggesting potential treatment targets.

Dermoscopy shows that varying hair shaft thickness and single hair follicles are main signs of male pattern baldness, especially in the fronto-temporal region.

The cat's skin condition improved and hair regrew after antifungal treatment.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Diphenylcyclopropenone (DPCP) effectively treated both alopecia areata and verruca vulgaris.

Oxidative stress may worsen female pattern hair loss and could help track the disease and treatment.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Older people's hair cuticles get more easily damaged and lose protective oils, especially in their 40s and 50s.

Dermoscopy is a useful tool for diagnosing female pattern hair loss.

Antifungal treatment can improve severe skin infections with cutaneous horns.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Hair growth and shedding are linked and can be disrupted, causing a delay known as the hair eclipse phenomenon, which is common in certain hair conditions and could lead to new treatments.

A boy had a rare scalp condition with thickened skin and different-colored hair.

Psoriasis causes changes in certain keratins and shrinks sebaceous glands in the scalp.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Middle-aged women with chronic telogen effluvium experience increased hair shedding but usually don't get significantly thinner hair.

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