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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

SPIOMET therapy may be a promising alternative to oral contraceptives for treating adolescent PCOS.

Plumbago zeylanica L. leaves may help dissolve blood clots and have antioxidant benefits.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Radiotherapy effectively treated a large scalp tumor in an elderly woman, avoiding surgery.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

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

Standardizing light therapy methods could improve spinal cord injury treatment.

Three genes linked to the development of trichilemmal cysts were found.

Platycarya strobilacea extract significantly improves hair growth and follicle health.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

A man regrew hair in 15 days using Pracchana and cupping therapy.

Orange spots in scalp trichoscopy can help diagnose scalp sarcoidosis.

The BASP classification is effective for diagnosing pattern hair loss in Indian men and women.

The PS-b-PAA copolymer nanomicelles are effective for delivering a cancer treatment drug in photodynamic therapy.

Systematic end-of-trial biopsies are the most reliable way to assess outcomes.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

The treatment combination is effective and generally safe for lung cancer.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

A rare ovarian tumor was successfully treated with surgery and chemotherapy.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Nanostructured lipid carriers can effectively deliver spironolactone to hair follicles for treating hair loss.