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Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Follicular Unit Transplantation is a reliable hair restoration method with a high success rate and minimal scarring.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Machine learning and deep learning can effectively diagnose alopecia areata.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

UV photography can help identify people at higher risk for skin cancer, and male pattern baldness at age 45 is linked to a higher risk of certain skin cancers.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concluded that FDA-approved treatments like minoxidil and finasteride are effective for hair loss, while the effectiveness of natural remedies and other non-approved treatments is not well-supported by evidence.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Skin aging reflects overall body aging and can indicate internal health conditions.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.