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Men with male pattern baldness have increased arterial stiffness.

Using dermoscopy to guide scalp biopsies is an effective way to diagnose cicatricial alopecia.

Most cutaneous adnexal tumors examined were benign and resembled common skin tumors.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

The document concludes that skin and nail changes can indicate various underlying health conditions.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

The study concluded that Frontal fibrosing alopecia can affect younger people, is often missed in men, and may be autoimmune-related.

New understanding of the causes of primary cicatricial alopecia has led to better diagnosis and potential new treatments.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Less than a quarter of alopecia areata cases were unusual forms or had paradoxical regrowth.

IL-1α levels are higher in alopecia areata patients, suggesting a role in the disease.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

The document suggests simplifying alopecia diagnosis and improving techniques for better accuracy.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Cornification is the process where living skin cells die to create a protective barrier, and problems with it can cause skin diseases.

The cat's skin condition was linked to cancer and did not improve with treatment, leading to a poor outcome.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

The visfatin GT genotype may increase the risk of Alopecia Areata.

New materials and methods could improve skin healing and reduce scarring.

Current treatments for androgenetic alopecia manage symptoms but don't cure it, and it affects social and psychological well-being.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Scalp melanoma is more common and easier to diagnose early in people with androgenetic alopecia due to sun damage.

Apremilast may help treat lichen planopilaris and frontal fibrosing alopecia when other treatments fail.