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Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

People with lichen planopilaris often have seborrheic dermatitis, which can delay the diagnosis of lichen planopilaris.

ALEP is a drug-triggered skin reaction with pustules that clears up in a week after stopping the drug.

Early recognition of loose anagen hair syndrome is important to prevent misdiagnosis and unnecessary treatments.

Higher fluence low-level laser therapy effectively promotes hair growth in androgenetic alopecia, with varying effects based on sex.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Lipase H is important for hair follicle function and shaping hair fibers.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Lyophilized platelet-rich plasma is beneficial and effective for various medical treatments, including tissue regeneration and hair regrowth.

Linear cutaneous lupus erythematosus on the scalp is rare, often affects young Asians, and can be treated with specific medications.

The mTOR pathway proteins are altered in the hair follicles of patients with Lichen Planopilaris and Frontal Fibrosing Alopecia.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Lanyu pigs show that partial-thickness wounds can partially regenerate important skin structures, which may help improve human skin healing.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The Laxometer helps make hair transplants with many grafts safer.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

LLLT promotes hair growth and improves hair density safely in men and women.

JAK inhibitors may help treat certain types of hair loss, but more research is needed.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

PP405 may help hair growth by activating hair follicle stem cells.

The research identified specific genes that are active in the cells crucial for hair growth.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

pCLCA2 protein may help maintain skin structure and function.

Oral retinoids may help some patients with hard-to-treat lichen planopilaris, but more research is needed.