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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

The "flying-wings" scalp flap technique is a simple, safe, and effective way to reconstruct large areas of scalp loss in children.

A woman had eye pain and vision loss after a hair growth treatment, but her symptoms improved after a month.

A 15-year-old boy's severe scalp condition improved significantly with adalimumab and baricitinib treatment.

Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.

The authors updated the criteria for diagnosing frontal fibrosing alopecia, making it easier to diagnose without a biopsy.

Two patients with lupus had an unusual type of hair loss not typical for the disease but improved with treatment.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A six-year-old girl with extra hair on her elbows was treated with hair removal methods.

Forehead rejuvenation is key to facial rejuvenation, with various surgical techniques tailored to individual needs.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Hair shaft changes may be linked to CCCA, but their role is unclear.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Early scar classification in lupus can improve treatment and patient outcomes.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Corticosteroids can reduce scarring in acne keloidalis by targeting specific cells.

Hair transplants can rarely cause scalp inflammation leading to hair loss, needing early detection and treatment.

Perifollicular elastolysis is poorly understood, with limited treatment options and inconsistent results.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.