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

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document is a detailed medical reference on skin and genetic disorders.

Patients with acanthosis nigricans often have insulin resistance and signs of increased male hormones, but treatment targeting these male hormones is generally ineffective.

Women with Systemic Lupus Erythematosus should have closely monitored pregnancies and avoid certain medications to improve their pregnancy outcomes.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

The document concludes that diagnosing hair loss requires evaluating multiple histological features, as no single feature is definitive on its own.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

Hair loss in elderly women is often caused by various factors, including hormonal changes after menopause.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

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

Studying rare genetic disorders can help us understand and treat common diseases better.

The conclusion is that there's a link between high testosterone levels, insulin resistance, and certain skin conditions, regardless of obesity.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

The twins' condition is unique and doesn't match any known syndromes.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Studying acne-related syndromes helps us understand acne causes and can lead to new treatments.

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