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Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

FPHL causes hair loss in women due to genetics and hormones; minoxidil and anti-androgens are treatments, and early intervention is advised.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

PRP treatment may promote hair growth and improve hair density in women with AGA, but more research is needed.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

No clear link between specific gene and hair loss in Mexican brothers.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Experts recommend using evidence-based methods to diagnose and treat hirsutism, focusing on symptoms and underlying causes.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

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

Aromatase gene variation may increase female hair loss risk.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

AR polyglycine repeat doesn't cause baldness.