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Vitiligo is linked to autoimmune diseases and hearing issues, so hearing tests are recommended for patients.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Alopecia areata involves immune response and gene changes affecting hair loss.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Plant-based remedies may treat hair loss by reducing inflammation and improving insulin resistance.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

AGA is a common hair loss affecting both genders, treated with various therapies to promote regrowth and slow thinning.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

FFA's causes may include environmental triggers and genetic factors.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

At least 87% of Indian men experience hair loss, with type II being most common and severity increasing with age.

Daughters of women with PCOS generally experience normal puberty but may have more body hair and different body fat distribution.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Hairless gene not strongly linked to baldness.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.