Search

everythinglearnresearchcommunity

for

Search:↓

Activating Nrf2 can help protect against hearing loss.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Fibrinogen/LDL apheresis may improve speech perception in sudden hearing loss, especially for those with high fibrinogen and LDL levels.

Low Level Laser Therapy may improve noise-induced hearing loss.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

4-octyl itaconate may prevent hearing loss caused by the drug cisplatin by activating certain cell protection pathways.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Stem cell therapy is promising for treating various health conditions, but more research is needed to understand its full potential and address challenges.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

New treatments for hair loss may target specific pathways and generate new hair follicles.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

COVID-19 leaves 80% of patients with long-term symptoms like fatigue and headaches.

The NAMS 2014 recommendations guide healthcare providers on treating health issues in midlife women, emphasizing individualized care and informed decision-making.

The document suggests using natural remedies like bloodletting and honey for various health issues but lacks scientific evidence for their effectiveness.

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

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document is a detailed medical reference on skin and genetic disorders.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.