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Cantú syndrome may be linked to pituitary adenomas.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Visible light can damage skin and most sunscreens don't block it well; more research is needed on its effects and protection methods.

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

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

PRP with microneedling improves hair growth and patient satisfaction more than injections for androgenetic alopecia.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

FGF13 gene changes cause excessive hair growth in a rare condition.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

People with common hair loss conditions may have a higher risk of heart disease and related health issues.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Dihydrotestosterone and 5α-Reductase play a role in hair loss and prostate health, and finasteride can increase hair growth in men without affecting sperm production, but it doesn't work for postmenopausal women with hair loss.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Minoxidil, originally a blood pressure medication, is effective in treating hair loss in men and women, with different strengths recommended for each.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.