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The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

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 review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

The document explains different hair and scalp conditions and their treatments.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

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

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

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

Light microscopy is useful for diagnosing different hair disorders.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Using special RNA to target a mutant gene fixed hair problems in mice.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

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

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

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

TGM3 is important for skin and hair structure and may help diagnose cancer.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document concludes that diagnosing female hair loss requires careful examination, with treatments varying by condition and psychological support often necessary.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

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

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.