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The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

Puberty often causes skin issues like acne and excessive sweating, and treatments require patience as results may vary.

Male pattern baldness is an unintended side effect of the body's use of androgens for muscle growth, especially in those genetically prone to it.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

The document explains various skin conditions and their treatments.

People with advanced chronic kidney disease often have skin problems, which can be treated with various medications and procedures to improve their quality of life.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

The document recommends all three dermatology books for a library, noting their detailed content but also suggesting improvements in clarity and consistency.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

FFA's causes may include environmental triggers and genetic factors.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.

Minoxidil and Finasteride are effective for male baldness; more research is needed for hair aging treatments.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

People with common hair loss conditions may have a higher risk of heart disease and related health issues.

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

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Skin issues can indicate immune system problems.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.