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A rare case of a transplant patient developing a skin condition linked to HPV-49.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

People with atopic dermatitis have more CD4+ T cells that respond to a certain bacterial lipid, which may play a role in the skin condition's inflammation.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

Some patients who had a severe drug reaction developed long-term hair loss.

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

PAS III can cause multiple autoimmune diseases with noticeable skin issues.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Prednisone may cause multiple skin nodules in lupus patients.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

Consider Castleman's disease in similar cases; histology and steroids help diagnose and manage it.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

SLE should be considered in unexplained fevers, even in males.

Prednisone reduces organ mast cell infiltration but does not alter the abnormal appearance of mast cells in systemic mastocytosis.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

An addax had skin cancer that spread to lymph nodes and was euthanized.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

A patient in Portugal with chronic pulmonary histoplasmosis had a complex medical history and environmental exposures.

The patient has a rare skin condition that shows features of two known disorders.

A new skin disease in four Labrador retrievers responded well to immunosuppressive treatment.

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.