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Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.

Pulsed dye laser treatment was effective for a skin condition resistant to other treatments.

Restoring immune privilege in hair follicles could help treat certain types of hair loss.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Renal histology is crucial for diagnosing simultaneous SLE and IgG4RD.

Permanent hair loss after a stem cell transplant can be a sign of chronic immune system attack on the scalp.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Early detection and histopathology are crucial to prevent permanent hair loss in cicatricial alopecia.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Intralesional cidofovir might be a good alternative treatment.

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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Leukemia should be considered in teens with unexplained bleeding.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Lichen planopilaris patients are more likely to have hypothyroidism.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

Innate lymphoid cells type 1 may contribute to alopecia areata.

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Skin issues from chronic graft-versus-host disease greatly affect daily life, needing teamwork between blood and skin doctors.

A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

Tislelizumab can cause cutaneous lupus erythematosus.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

ILC1-like cells can independently cause alopecia areata.