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The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

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."

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Bimatoprost is safe and effective for improving eyebrow hair.

Early diagnosis is crucial for treating alopecia effectively.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Immune cells are essential for early hair and skin development and healing.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

Assessing newborn scalp hair can reveal important health information.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.