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Hair bands are a new symptom of facio-genito-popliteal syndrome.

Managing side effects of endocrine therapy is crucial to improve adherence and survival in breast cancer patients.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

Urologists should monitor mental health in patients taking finasteride due to potential links to suicidal thoughts, adjusting dosage or stopping use if necessary. More research is needed to confirm if finasteride causes these thoughts.

Newborn mouse skin cells can grow hair and this process can be recreated in adult cells to potentially help with hair loss.

Certain immune system proteins are important for skin healing but can cause problems if there are too many of them.

Wound healing insights can improve regenerative medicine.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

The study suggests that the arrector pili muscle is important for hair health and its damage might contribute to hair loss.

Stem cell research and regenerative medicine have made significant advancements in treating various diseases and conditions.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Ectomesenchyme is a key source of skin stem cells.

Obese women with PCOS are more likely to have fatty liver disease.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

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

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

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.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

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

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.