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An 80-year-old man's deep beard infection was cured with oral terbinafine after identifying the fungus Trichophyton verrucosum.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

Lack of KSR1 stops certain skin tumors in mice.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Fungal infections like ringworm affect skin, hair, and nails in humans and animals, requiring culture for diagnosis and specific treatments.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Timely treatment with antibiotics and antiretrovirals can significantly improve health in HIV patients with syphilis.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

A man developed a skin cancer called folliculotropic mycosis fungoides after a kidney transplant.

Malassezia in cat skin biopsies may indicate internal cancer.

The skin issues in the two dogs might be caused by infection or self-injury, not genetics.

T-cell patterns in skin help distinguish alopecia areata from androgenetic alopecia.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

Anti-Ro exposed children had more reported neuro-psychiatric issues, but differences from healthy controls were not significant.

Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

ATP-sensitive potassium channels play a role in chloroquine-induced itch in mice.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

A liver transplant patient with APECED had a rare VZV recurrence and pneumonia, treated successfully, but later died from other infections.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

Syphilis can cause unusual symptoms like hair loss and joint pain, but treatment is effective.

Tinea capitis in Benghazi mainly affects children under 10, with Trichophyton violaceum as the leading cause.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

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