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A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Two new gene mutations cause a rare hair disorder.

New treatments for lupus show promise, but more research is needed, especially for children.

Methotrexate is best for lichen planopilaris, and retinoids are best for frontal fibrosing alopecia, but side effects are common.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

Early recognition and a multidisciplinary approach are crucial for effectively managing complex autoimmune conditions like SLE with CAPS and AHA.

Scarred skin in lichen planopilaris loses immune cells due to a decrease in a specific protein in skin cells.

Linear Discoid Lupus Erythematosus of the scalp can cause hair loss and should be considered in similar cases.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

A child with a rare scalp condition regrew hair after treatment.

A horse with severe hair loss was diagnosed with alopecia areata and a yeast infection.

The study concluded that people with Lichen Planopilaris have a more diverse scalp bacteria and different metabolic pathways compared to healthy individuals.

Mycophenolate mofetil effectively improved skin pigmentation and itching in a woman with lichen planus pigmentosus and frontal fibrosing alopecia.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

KLHL24-mutant stem cells help understand skin and heart disease.

A woman was wrongly diagnosed with lupus but actually had leprosy.

Managing multiple autoimmune diseases in one patient is very challenging.

Lichen planopilaris may have a genetic link.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

Managing frontal fibrosing alopecia and lichen planus pigmentosus is challenging due to resistant hair loss and skin discoloration.

New treatments targeting specific genes show promise for treating keratin disorders.

Flexural follicular lichen planus is a rare skin condition affecting body folds.

The conclusion is that certain scalp tissue changes are characteristic of lichen planopilaris, with mucinous perifollicular fibroplasia being a new feature for diagnosis.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.