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Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

The document concludes that treatments for female hair loss and excessive hair growth are temporary and not well-studied.

Hair amino acid levels can indicate metabolic disorders.

A new mutation in the HR gene causes hair loss in a specific family.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document suggests a need for collaboration, better evidence, and a responsible framework to safely and effectively advance regenerative therapies to clinical use.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Early diagnosis and treatment, like topical minoxidil, can prevent hair loss in children.

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

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Severe acne in a young girl may indicate underlying hormonal issues.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

New treatments for hair growth disorders are needed due to limited current options and complex hair follicle biology.

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.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.