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A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Ossification in trichilemmal cysts is more common than previously believed.

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

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Human hair has electromagnetic properties.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

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

Human hair and mouse whiskers emit similar biomagnetic fields.

Alopecia areata and lichen planus can occur together in children, which is important for diagnosis and treatment.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A man had temporary hair loss from radiation during a medical procedure but regrew his hair after treatment with minoxidil lotion.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Loose anagen hair can appear at any age and may improve over time.

Human hair's biomagnetic fields can affect blood cell clumping and coagulation.

KLHL24-mutant stem cells help understand skin and heart disease.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Microneedling with platelet-rich plasma can cause temporary, painful lymph node swelling in some patients.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

Dermoscopy can non-invasively detect eruptive vellus hair cysts on the labia majora.

There's an urgent need for better treatments for hair loss caused by radiation therapy.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

The girl's skin condition is benign but challenging to treat due to its size and location.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Two cows had a rare hair disorder causing hair loss but were otherwise healthy.