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sPLA2-X is crucial for normal hair growth and follicle health.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The conference concluded that understanding hair and nail disorders is important, iron deficiency may be linked to hair loss, and while some treatments for skin conditions are effective, they may have risks and high costs.

Thyroid hormones affect skin texture, hair and nail growth, and can cause skin diseases related to thyroid problems.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

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.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

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

Liposomes improve drug delivery and reduce skin irritation in dermatology.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The research found specific genes and pathways that control fur development and color in young American minks.

Skin problems are common after stem cell transplants, and early treatment by dermatologists can improve patient outcomes.

The document explains how to identify different hair problems using a microscope.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

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

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.