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Chinese patients with primary cicatricial alopecia often have folliculitis decalvans, benefit from treatment, but may experience relapse, with dermoscopy being a useful diagnostic tool.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A new DSG4 gene mutation causes hair defects in a young girl.

Women with skin conditions who have body image concerns often experience mental health issues and a lower quality of life.

Selenium disulfide shampoo effectively reduces dandruff and is well-liked by users.

People with celiac disease have a higher risk of developing alopecia areata.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

5α-reductase deficiency can cause ambiguous genitalia and gender dysphoria, treatable with testosterone.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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 baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

Low-dose chemotherapy is safer, more effective, and cost-effective than surgery for treating bone lesions in children.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

SLE and DM can coexist but are rare and need careful evaluation.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.