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Timely diagnosis and treatment of complex autoimmune diseases like APS2 are crucial to prevent complications and improve life quality.

Danon disease can be hard to diagnose due to non-specific symptoms.

Hepatitis C treatment may cause frontal fibrosing alopecia.

Lower 2D:4D finger ratios in HS patients suggest prenatal hormone influence on the disease.

A pineal tumor caused a boy's early puberty, which changed from peripheral to central after treatment.

Human placenta helps hair grow back after chemotherapy by blocking cell death and increasing hair follicle growth.

Hair dye ingredient PPD can cause severe allergic reactions, including facial swelling.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.

Most hirsutism patients had idiopathic hirsutism or PCOS, with hormonal imbalances and signs like acne and irregular periods.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

HBM-based nursing intervention improved medication compliance, reduced negative emotions, and enhanced quality of life for renal transplant recipients.

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

Human scalp hair follicles can be used to study how prolactin affects hair growth and cell death.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Early diagnosis and multidisciplinary care are crucial for managing PCOS in adolescents.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

Inflammation and fibrosis are not significantly different in pattern hair loss compared to controls.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

The patient had paraneoplastic pemphigus without mucosal involvement.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

Researchers found a new mutation causing total hair loss from birth.

The man has a genetic skin condition called pachyonychia congenita.