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A woman with discoid lupus improved with treatment after being misdiagnosed with a different hair loss condition.

Zinc deficiency was the real cause of the boy's symptoms, not a skin infection.

Most pregnancies with SLE resulted in intrauterine growth restriction (IUGR).

Chinese patients with systemic lupus erythematosus commonly experience oral ulcers, arthritis, alopecia, skin rash, and nephritis.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

A 38-year-old African American woman has a rare condition that prevents her from growing long hair.

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

A girl with lupus had unusually long and thick eyelashes, a rare symptom of her condition.

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

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.

The patient's scalp lesions stabilized with a combination of treatments after initial therapies failed.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

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

Doctors often diagnose Cushing's syndrome late, which worsens symptoms; earlier detection is needed.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

Serine is vital for hair follicle stem cells to balance hair growth and skin repair.

Some people experience lasting sexual, psychological, and sleep problems after using finasteride or SSRI antidepressants, possibly due to similar underlying causes.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

Biotin, alone or with minoxidil, effectively treats short anagen syndrome.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

The document concludes that early diagnosis of Balint's syndrome is crucial for effective treatment and that understanding drug interactions, like between ritonavir and statins, is important for patient care.

Loose anagen hair syndrome causes easily pulled, thin hair in kids but is harmless and temporary.