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Deep learning helps detect skin conditions and is advancing dermatology diagnosis and treatment.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Researchers isolated a new type of stem cell from mouse skin that can renew itself and turn into multiple cell types.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

The meeting discussed medical findings, including benefits of certain treatments for cancer and heart conditions, and highlighted issues like poor adherence to preventive measures and skill gaps among interns.

The document concludes that early recognition and treatment of primary cicatricial alopecia is crucial to prevent permanent hair loss.

Finasteride increases hair density in female androgenetic alopecia, but individual results may vary.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Genetically-altered adult stem cells can help in wound healing and are becoming crucial in regenerative medicine and drug design.

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

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.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

CD4+ skin cells may be precursors to basal cell carcinoma.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The document explains various skin conditions and their treatments.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

IL-2 treatment causes skin eruptions and other reversible side effects, and may play a role in psoriasis.

The EDAR gene greatly affects hair thickness in Asian populations.

Wool and hair fibers absorb moisture similarly due to their keratin structure, with the amount of non-crystalline areas affecting the moisture uptake.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Keratin fibrils in hair form and stop growing at specific points in the follicle.

Men, diabetes, and high inflammation levels lead to higher COVID-19 antibodies.