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Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The research found that specific stem cells maintain skin gland openings and that disrupting their activity can cause blockages or early cancer signs, indicating a need for targeted treatments.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

Most women have a widow's peak and specific hairline features useful for designing hair restoration surgery.

Trapezoid donor strips give more hair follicles than elliptical ones in hair transplants.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Intracorneal vacuoles are common in parakeratotic skin diseases in dogs, especially with more parakeratosis.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Variation in the TCHH gene affects wool curliness in sheep.

A new classification for depth control in hair restoration surgery was proposed, dividing it into three grades based on the depth required for successful graft extraction.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

3D virtual planning can help in precise skull reconstruction for advanced skin cancer, but patient-specific factors must be considered.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Occipital scalp affects female hair loss; terminal/vellus ratio helps diagnose androgenetic alopecia.

Early minipulse corticosteroid therapy can effectively treat scalp discoid lupus in children.

Nevus comedonicus can appear later in life and affect both eyelids.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Dermoscopy is a useful tool for diagnosing and managing topical steroid dependent face.

SOX9 is essential for the development of various organs and hair follicles.

The girl's symptoms suggest a complex condition that's hard to diagnose despite normal test results.

Extramammary Paget disease can spread deeply into tissues, reaching up to 3.6 mm.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

Exclamation mark hairs help distinguish syphilitic alopecia from alopecia areata.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

Neck burn scar contracture recurrence is more likely with larger neck defects, and closer follow-up can help detect it sooner.