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The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Mechanical trauma like towel drying can cause knotted hair even in straight hair.

Hair microscopy is a useful and affordable way to diagnose hair disorders.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

OCT can effectively examine and reveal details about human hair and scalp conditions.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Excessive blow-drying can cause "bubble hair," leading to hair loss and fragility, but improves when heat use is reduced.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Monilethrix causes fragile, patchy hair loss.

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

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

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.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Shaving and avoiding brushing improved the patient's beard hair condition.

The document concludes that accurate diagnosis of hair disorders is crucial and requires a range of diagnostic methods.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

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

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Alopecia Areata causes significant structural and compositional changes in hair.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.