Search

everythinglearnresearchcommunity

for

Search:↓

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

Hair follicles produce and respond to melatonin, affecting hair growth and sensitivity to estrogen.

Zebrafish larvae are used to study and find treatments for ear cell damage because they are easier to observe and test than mammals.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The document is a detailed medical reference on skin and genetic disorders.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Long-term high testosterone levels can improve bone density and reduce body fat but may increase the risk of prostate cancer and high blood pressure.

Increased free testosterone can lead to stronger bones and less body fat but also higher risks of prostate cancer, hair loss, spine issues, and high blood pressure.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

New treatments for hair loss are being developed using both traditional Chinese and Western medicine.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

Human hair shows promise for non-invasive medical testing, but more research is needed to standardize its use.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

The document concludes that hair is complex, with a detailed growth cycle, structure, and clinical importance, affecting various scientific and medical fields.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

The document concludes that understanding how hair follicles naturally die and regenerate is important for insights into organ development and could impact health and disease treatment.

Feather growth and regeneration involve complex patterns, stem cells, and evolutionary insights.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.