Search

everythinglearnresearchcommunity

for

Search:↓

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Mesenchymal stromal cells may help treat severe COVID-19, but more research is needed to confirm their effectiveness.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

Women with PCOS often have mood disorders and a lower quality of life, and treatment should focus on both physical and mental health.

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.

Obesity worsens Polycystic Ovary Syndrome symptoms, and weight loss is a key treatment.

Hormonal therapies are safe and effective for treating acne in female adolescents, with specific treatments for those with endocrine disorders.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

Different combinations of human hair keratins affect how hair fibers form.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.