Search

everythinglearnresearchcommunity

for

Search:↓

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

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Microneedle arrays with nanotechnology show promise for painless drug delivery through the skin but need more research on safety and effectiveness.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Dermoscopy is useful for diagnosing various skin, hair, and nail disorders and can reduce the need for biopsies.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Skin organoids are a promising new model for studying human skin development and testing treatments.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

New treatments for psoriasis have improved effectiveness and may reduce long-term side effects when combined with standard therapies.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Further research is needed to improve hair regeneration using stem cells and nanomaterials.

Hair loss patients have different microbes in hair follicles, possibly affecting hair loss.

New melanoma treatments can cause skin side effects, including skin cancer and rashes, but combining treatments may reduce these risks.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

The PCOS-specific questionnaire needs more work to fully measure quality of life in clinical trials.

The document concludes that veterinary dermatologists need more experience and a better approach to treating skin diseases in nonhuman primates.

The Arabic Skindex-16 is a reliable and valid way to measure the impact of skin conditions on quality of life in Saudi patients.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Finasteride improves hair growth and reduces hirsutism in women, but side effects and optimal dosages need further research.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Yellow and orange colors are important for diagnosing certain skin conditions.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.