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The conclusion is that teeth, hair, and claws have similar stem cell niches, which are important for growth and repair, and more research is needed on their regulation and potential markers.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

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

Hair changes can indicate systemic diseases or medication effects.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

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

Dlx3 is essential for hair growth and regeneration.

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

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

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

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

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Scientists created stem cells that can grow hair and skin.

Trichoscopy and trichogram are useful for diagnosing hair and scalp conditions.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases by their unique visual features.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

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

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

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

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

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

NF-κB is crucial for different stages and types of hair growth in mice.

mTORC1 activity is important for hair growth and color, and targeting it could help treat hair loss and greying.

The ingredients could help prevent hair loss by promoting hair growth and increasing VEGF secretion.