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A 16-year-old girl with autoimmune hemolytic anemia and deep vein thrombosis improved with treatment, possibly indicating systemic lupus erythematosus.

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

Lupus can cause unusual vision problems, so it's important to consider it in such cases.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Oral ulcers are common in SLE patients and often link to other symptoms.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Janus kinase inhibitors show promise for treating alopecia areata but need more research for confirmation.

A 16-year-old boy with Castleman's disease and lupus was successfully treated and showed no recurrence.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Skin problems are common in lupus, important for diagnosis, and can be triggered by sunlight.

A 69-year-old man with sinus infection and fainting spells was diagnosed with a rare kidney disease, treated with steroids and a specific drug, which improved his condition.

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

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

The text talks about a rare skin condition causing hair loss and suggests that people with this should also check their lung and heart health.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

IV cyclophosphamide effectively treated severe lupus nephritis in Indian patients, but longer follow-up is needed.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

JAK inhibitors help with skin conditions but need more research on dosing and safety.

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

Japanese vitiligo patients and their families often have other autoimmune diseases.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A woman with thymoma developed a rare chronic condition similar to graft versus host disease after surgery.

A woman's hair loss led to discovering she had lupus.

Azathioprine treatment led to rapid hair regrowth in a woman with alopecia universalis.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Distinguishing drug-induced lupus from systemic lupus is challenging and requires careful monitoring.