Search

everythinglearnresearchcommunity

for

Search:↓

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

AR gene not major factor in female hair loss; different from male hair loss.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Finasteride side effects in young men may be linked to specific gene variations.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

Adrenal disorders can cause lasting brain and behavior issues in children.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Hormonal imbalances, often indicating conditions like PCOS, are common in women with hard-to-treat acne, and a treatment approach addressing these imbalances may be needed.