Search

everythinglearnresearchcommunity

for

Search:↓

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Two women with darker skin had both frontal hair thinning and skin discoloration.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Lichen planopilaris can be accurately diagnosed and effectively treated.

Lipin-1 is important for skin cell differentiation and skin barrier function.

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.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

Mycophenolate mofetil may improve symptoms and stop hair loss in Lichen planopilaris, but more research is needed.

Lipocartilage is a new type of tissue that affects hair growth and cartilage regeneration.

The boy's symptoms suggest a possible new medical condition.

Lichen planopilaris and frontal fibrosing alopecia are likely distinct diseases with different tissue involvement.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

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

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Long-lived proteins may predict age-related diseases.

Danon disease can be hard to diagnose due to non-specific symptoms.

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

The document reports a rare case of ECCL with a new association with optic disc colobomas.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss in Discoid Lupus.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

A man had two rare autoimmune diseases that might be connected.

A unique case showed a rare combination of two types of lichen planus on the face.

Lichen planopilaris is the most common type of scarring hair loss observed, with a variety of symptoms and tissue changes.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

Increased blood vessel growth in lichen planopilaris may signal active disease needing aggressive treatment.

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