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Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A boy's hair, nails, and skin improved after 6 months of steroid treatment.

Recent progress has been made in understanding inherited hair and nail disorders.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Treatment improved symptoms in a woman with HAIR-AN syndrome.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Epilation and DHT cause skin calcification by increasing ATP and calcium deposits.

Fatp4 is crucial for healthy skin development and function.

A 14-year-old boy was diagnosed with a rare hair condition that may lead to hair thinning and has no known effective treatments.

A rare nail bed cancer was successfully treated with no recurrence after 4 years.

Self-induced hair loss should be considered in patients with androgenetic alopecia.

The woman's skin condition improved with specific oral and topical treatments.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Acitretin effectively improved the woman's skin condition.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Chronic Acrodermatitis Enteropathica can persist into adulthood and requires careful zinc treatment.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A man developed a rare late-onset hair-pulling disorder, usually seen in younger people.

Hair-related body dysmorphic disorder is common in hair loss patients and needs early recognition for proper treatment.

Disruptions in Wnt signaling can lead to skin and hair diseases.

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

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.