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Mutations in the P2RY5 gene cause hereditary woolly hair.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

Hair loss in women is often due to hereditary conditions or stress, and while treatments like minoxidil can help, diagnosis and management require medical guidance.

The two-factor model fits better for Chinese patients' understanding of illness causes than the original four-factor model.

The document explains different hair and scalp conditions, including common hair loss after pregnancy or illness, drug-induced hair loss, hereditary excessive hair growth, patterned baldness, autoimmune hair loss, and permanent loss due to skin disease, with generally limited treatment options.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Some African American women's central scalp hair loss is linked to genetics and past fungal scalp infections, with more research needed on other causes.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

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

Using a scalp flap for hair transplantation gives denser, faster results than older methods, but it's complex and needs careful planning.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

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

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document concludes that while some hair and scalp disorders can be treated, hair loss from destroyed follicles is permanent, and damaged hair can only regrow naturally.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Combining trichology and homeopathy is effective for diagnosing and treating hair loss.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

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

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Common baldness is a hereditary condition that can be treated with medications or surgery to prevent progression and improve self-esteem.

Light therapy might help treat hereditary hair loss by improving hair follicle growth in lab cultures.