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Metabolic issues may trigger lymphocytic cicatricial alopecia, and treatments targeting these issues could help.

A high fat lard diet may protect against skin fibrosis and affect hair growth.

A leukemia patient showed skin peeling similar to kwashiorkor, a severe protein deficiency.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

Anti-phospholipid antibodies in SLE can cause thrombosis and bone necrosis.

Treatment improved some symptoms but not all.

Early recognition and treatment of LPP can prevent hair loss and improve quality of life.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Lymphoma should be considered in unusual scalp hair loss cases, as treatment can work but may lead to severe complications.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

Blocking autophagy worsens lipid buildup and dysfunction in brain cells after injury.

A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

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

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

Anterolateral leg alopecia is a benign, nonprogressive hair loss condition on the lower legs that is not well understood and may resolve on its own.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

A pancreatic tumor caused high glucagon levels and symptoms, but treatment reduced glucagon and shrank liver tumors.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

A fungal skin infection was successfully treated with medication and compression therapy.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

A 6-year-old Asian boy has a rare scalp condition causing hair loss and thickening, with unclear causes and no effective treatment.

Early diagnosis of leprosy is crucial to prevent disabilities and spread, even in non-endemic areas.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Human hair follicles have a unique way of using energy and might use the Cori cycle; blocking CCR5 could help treat hair loss.