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

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

Acne can be managed with various treatments and requires psychological support due to its emotional impact.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

The document explains various skin conditions and their treatments.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Hirsutism and acanthosis nigricans are reliable skin signs of PCOS and suggest the need for further tests for related health issues.

Hirsutism and acanthosis nigricans are reliable skin signs of PCOS linked to metabolic issues, while acne is not a reliable marker of the condition.

Women with PCOS often have more hair growth, skin darkening, and acne, which are linked to hormonal and metabolic issues.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

People with advanced chronic kidney disease often have skin problems, which can be treated with various medications and procedures to improve their quality of life.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

Lupus can cause different skin problems, and treatments like quitting smoking and using certain creams or medicines can help.

The document concludes that different types of hair loss have specific treatments, and early diagnosis is crucial for preventing permanent hair loss.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

A pregnant woman's skin condition improved after giving birth, possibly due to high estrogen levels during pregnancy.

Hair loss caused by longer latent hair cycle and sudden miniaturization, not gradual follicle size reduction.

There are many treatments for common hair loss, but more trials are needed to decide which are best.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.