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About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Gut bacteria overgrowth may cause some Post-Finasteride Syndrome symptoms.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

A CCS patient with severe complications was successfully treated using combined therapies.

Microbes in the small intestine may cause Post-Finasteride Syndrome symptoms.

A Pomeranian dog had rickets due to a new gene mutation, leading to severe symptoms and euthanasia.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

A potential genetic link between Werner syndrome and kidney disease was suggested.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

Looking at skin can help find and treat serious diseases early.

FLCN helps control iron levels in cells.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A 13-year-old girl with various symptoms was successfully treated for autoimmune disease using the antibiotic co-trimoxazole.

A baby with KID syndrome died from infections and organ failure at 18 months old.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe side effects.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

COVID-19 may trigger severe skin flare-ups in people with autoimmune conditions like lupus.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.