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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.

Using neurohormones to control keratin can lead to new skin disease treatments.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Understanding proteins in skin structures like claws and hair is crucial for future research.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Some drugs can cause hair loss or increase hair growth, but these effects are usually reversible when the drug is stopped.

Certain transporters are found in human hair follicles and may affect hair growth and loss.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Pediatric transplant patients often experience unique skin changes mainly due to medication use.

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

Topical vitamin D is effective in treating vitiligo with few side effects.

The document concludes that while finding animal models for the skin disease Hidradenitis suppurativa is challenging, certain mouse mutations may provide useful insights for research and drug testing.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

Topical vitamin D is useful for some skin conditions but not effective for others, and more research is needed.

Triparanol therapy can cause hair loss and skin dryness without inflammation or damage to hair follicles or skin structures.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Patients on long-term hemodialysis often experience severe itching and various skin and nail problems.

Dermatological conditions are complex and treatments often have mixed results.

Retinoids can help treat skin disorders by improving the skin's outer layer.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The four patients have a unique type of ichthyosis affecting hair follicles.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Newborns with ichthyosis need specific care based on their skin type.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.