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Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

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

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The document concludes that combination therapy is most effective for treating excessive hair growth in women with idiopathic hirsutism, and more research is needed to understand the condition.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

The foreword introduces a medical issue discussing male hormonal health, treatments, and the effects of conditions like obesity and aging.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

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

10.5% of sheep in Ismailia, Egypt, had Sarcoptes scabiei, causing skin issues.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

Use minoxidil for hair loss treatment; assess results after 6 months.

Intralesional therapy for keratoacanthoma is effective and has fewer side effects than systemic treatments.

Some new isatin compounds could be strong cancer-fighting drugs because they fit well in cancer-related proteins and have good drug-like properties.

The new microrhizotron tool effectively observes and measures pepper plant roots non-destructively.

Researchers found four key stages of cell development that are important for hair growth and shedding in cashmere goats.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

The study mapped yak skin cells to understand hair growth better.

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

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

New treatments for hair loss are showing promise due to better understanding of genetics and the immune system.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

Researchers concluded that safe hair follicle extraction limits in FUE vary by individual characteristics and proposed a method to calculate these limits to maintain appearance.