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A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Kawasaki Disease is rare and often missed in adults, who show different symptoms than children, and may benefit from early treatment.

The document concludes that understanding the anatomical changes of the ageing face is important for effective rejuvenation treatments.

Hair can indicate early signs of metabolic disorders, with issues like protein deficiency stopping hair growth.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Ayurvedic treatment improved symptoms and reduced TSH levels in a hypothyroidism patient.

CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

The guidelines recommend informed consent for gender-affirming treatments and stress the importance of personalized, culturally sensitive care for transgender individuals.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

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.

The guidelines suggest a detailed approach to diagnosing and treating lupus, with a focus on regular check-ups, personalized medicine, and a range of drug options for different cases.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Eclipta alba extract improved learning, memory, and stress-related ulcers in rats without affecting movement or causing anxiety.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Postinflammatory hyperpigmentation causes dark skin patches and needs personalized treatment.

Hair mineral analysis might help diagnose diseases early, but standard methods are needed.

Vitiligo affects overall health and self-esteem, needing more research and awareness.

The treatment combining docetaxel, cisplatin, and 5-FU is feasible and effective for advanced head and neck cancer.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.

Hair grays due to oxidative stress and fewer functioning melanocytes.

Wnt signaling is crucial for skin and hair development and its disruption can cause skin tumors.