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A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

Ulcerative colitis involves immune activation, chronic inflammation, and metabolic issues, some of which persist even during remission.

Taste disorders in Cronkhite-Canada syndrome are severe in the front of the tongue but improve with treatment.

Macrophages play a crucial role in skin wound healing, with their numbers and sizes changing over time.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Panitumumab treatment can cause unusual hair growth in some colorectal cancer patients.

Hairless mice are more vulnerable to Listeria infection, but gut microbiota can help reduce damage.

A rare genetic condition can mimic symptoms of other diseases, making diagnosis challenging.

Leukokoria can signal Coats disease or other retinal issues, requiring early detection to prevent severe outcomes.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Cytarabine can cause multiple organ toxicities, especially neurotoxicity, but better research methods are needed to fully understand and predict these effects.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Different bovine tissues show varying types of cytokeratins.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

The postnatal thymus has cells like mesenchymal stem cells that can become different cell types and help maintain thymus structure.

Alopecia areata involves immune system issues and specific cell types that disrupt hair growth, leading to hair loss.

Mitoxantrone is effective for treating acute leukemia, especially in older patients, with a lower risk of heart damage.

Accurate diagnosis is crucial to distinguish between PCOS and rare ovarian tumors in teens with similar symptoms.

Certain blood markers, especially MLR, can help diagnose alopecia areata.

Allopurinol may cause rare granulomatous microscopic colitis.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.