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

Rice water and hibiscus can help improve hair health and growth.

HIV-1 may cause increased stem cell death in hair follicles, leading to hair loss.

Telogen Effluvium is a hair loss condition where treatment involves identifying and managing its triggers.

Acne and increased body hair in teenage girls are normal but severe cases may need hormone evaluation and treatment can prevent diabetes linked to PCO.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

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.

The skin is the largest organ, protecting the body, regulating temperature, and producing hormones.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Auxin and ethylene hormones both work together and against each other to control plant growth.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Quantifying hair shape is better than using racial categories for understanding hair characteristics.

Angora goat hair grows faster and produces more protein than cashmere goat hair, and certain hormones and nutrients positively affect hair growth and protein synthesis.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

EGFR is essential for normal hair development and follicle differentiation.

Hair transplants help transgender patients look more like their gender identity, with different procedures for trans women and men.

Adult mouse skin contains stem cells that can create new hair, skin, and oil glands.