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K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

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.

The document does not determine if adults with aphallia are fertile.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

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

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Treatments for acute leukaemia lead to high remission rates, but relapses occur, requiring ongoing advancements in care.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

Deleting MED1 in skin cells causes hair loss and skin changes.

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

New genes and pathways are important for testosterone production and male sexual development.

The document explains how the male reproductive system works, its role in making testosterone, and how conditions like obesity can disrupt it, leading to low testosterone and fertility issues.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The follicular unit extraction method for hair transplants is a technique with benefits and drawbacks.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

Certain genes are linked to the risk of developing Alopecia Areata.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The scraggly mutation causes hair loss and skin defects in mice.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.