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The over-the-counter supplement DHEA could make COVID-19 worse, especially in diabetics and people with G6PD deficiency.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

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.

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

Early balding in young Indian men may indicate a higher risk of metabolic syndrome and potential heart disease.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

To diagnose hair loss, use a systematic approach including history, exams, and tests.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Corticosteroids, especially prednisone, improve short-term muscle strength in Duchenne muscular dystrophy but have manageable side effects.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

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

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Different body areas in mice produce different hair types due to interactions between skin layers.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Men with male pattern baldness are more likely to have unhealthy blood lipid levels, which could signal other health issues.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Balding people may have higher heart disease risk.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Platelet Rich Plasma (PRP) treatment is safe and effective for hair growth in people with androgenic alopecia, and can also help treat bacterial infections.

Early balding, premature graying, and hair thinning can predict heart disease in young Asian males.

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

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.