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A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Testosterone and dihydrotestosterone affect hair growth, and new techniques like the folliculogram help study it, but fully understanding hair growth is still complex.

Alopecia areata involves immune response and gene changes affecting hair loss.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

The document concludes that secondary syphilis cases are increasing and often misdiagnosed, pityriasis rubra pilaris can be distinguished from psoriasis by skin cell features, and different skin layers produce specific components during skin repair.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

PCOS is caused by both genetics and environmental factors like diet and obesity.

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

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Moderately high prolactin levels do not cause hair loss in women.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Common types of non-scarring hair loss have various causes and treatments, but more effective solutions are needed.

The study concluded that combination therapy with topical corticosteroids and hydroxychloroquine or finasteride is effective in treating Frontal fibrosing alopecia in Asians.

Dr. Vera H. Price's 1979 work emphasizes the importance of accurate diagnosis and personalized treatment for hair loss.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

EF and PXE not closely related.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

The document concludes that skin and nail changes can indicate various underlying health conditions.

Gene linked to common hair loss found, may lead to new treatments.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Men with common hair loss (AGA) are more likely to have metabolic syndrome, which increases heart disease risk. Early screening could help prevent heart disease. More research is needed to understand this relationship better.

Hair loss gene found on chromosome 3q26.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.