Search

everythinglearnresearchcommunity

for

Search:↓

Reactive lipids from aging cells change the extracellular matrix, affecting cell function and inflammation.

The treatment led to significant hair regrowth in a lupus patient.

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

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

A brown shadow seen in dermoscopy is a marker for lichen nitidus.

Mesenchymal stem cells from laser-assisted liposuction are as effective and safe as those from conventional methods for cell therapy.

Toxic epidermal necrolysis is a severe skin reaction often linked to drugs, requiring careful medication use and supportive care.

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

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.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

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

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

Woman with diabetes had hair loss due to rare ovarian tumor; surgery improved hair growth.

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.

Alopecia mucinosa on the face can be linked to mycosis fungoides, a type of lymphoma.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

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

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

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

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

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

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Immunological treatment improved both neuropathy and alopecia.