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

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

A rare scalp condition caused scarring hair loss in a woman, improved slightly with treatment.

Timely treatment of eosinophilic asthma in rheumatic disease patients can prevent organ damage.

Frontal fibrosing alopecia is a scarring hair loss condition mainly affecting older women, with no known cause and treatments that may help stabilize hair loss.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

A woman with an unusual pattern of hair loss was confirmed to have Frontal Fibrosing Alopecia and treated with specific medications.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

The treatment was not recommended due to limited effectiveness and significant side effects.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

A patient with a thick scalp and hair loss was correctly diagnosed with alopecia areata and a thick scalp fat layer, not lipedematous alopecia, and regrew hair after treatment.

FFA has higher long-term remission rates than LPP.

Frontal fibrosing alopecia is a poorly understood condition with increasing cases and unclear treatment effectiveness.

A 16-year-old girl with HAIR-AN syndrome was treated with lifestyle changes and medications to manage her condition.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

PRP patients show varied symptoms and need more research to understand related conditions.

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

Frontal fibrosing alopecia in Brazil mostly affects postmenopausal women, often linked with hypothyroidism and eyebrow hair loss.

The treatment helped reduce symptoms and stabilize the hairline in most patients with Frontal Fibrosing Alopecia, but hair regrowth was limited.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

More inclusive research is needed to effectively treat frontal fibrosing alopecia in Black patients.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.