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Platelet-rich plasma is tolerable for lichen planopilaris and doesn't worsen the condition, but its effectiveness is unclear.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Lichen planopilaris may be an autoimmune disease causing hair loss due to immune system issues in hair follicles.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Accurate diagnosis is crucial for effective treatment of similar hair loss conditions.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A certain gene variation can affect protein production and is linked to male pattern baldness.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

The thulium laser and PDRN injections effectively improved hair thickness in patients with pattern hair loss.

A new method improves platelet testing for heart disease patients.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.

Amyloid deposits linked to a type of protein may cause a unique pattern of hair loss by disrupting hair growth cycles.

TCHHL1 is a protein important for hair growth, found in hair follicles.

FFA's causes may include environmental triggers and genetic factors.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

ARHGEF3 is essential for proper hair follicle development in mice.

A girl had rickets due to a gene mutation affecting vitamin D response.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

The revised BASP classification for hair loss is less accurate and harder to use but could still be a viable option.

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

Low-dose naltrexone and platelet-rich plasma can regrow hair in lichen planopilaris.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Mutations in the LSS gene cause a rare type of hereditary hair loss.