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Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The conclusion is that analyzing RNA from skin oils is a promising way to understand skin diseases.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.

Pica disorder in central Iraq is mainly found in females and is linked to low iron levels; treatment with iron improves most patients.

EdnrB signaling helps melanocyte stem cells regenerate and could be targeted to treat pigmentation issues.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Certain types of T cells are essential for healthy skin and play a role in skin diseases, but more research is needed to improve treatments.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Exosomes from umbilical cord cells fix hearing loss and damaged ear hair cells in mice.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Active oxygen species might be involved in skin tumor growth, but their exact role is unclear.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

OCT can effectively screen and diagnose various medical conditions non-invasively.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

Oxidative stress is a key factor in the development of Polycystic Ovary Syndrome, and weight management can improve symptoms.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

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

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

The telogen phase of hair growth is active and important for preparing hair follicles for regeneration, not just a resting stage.

The skin's basement membrane has specialized structures and molecules for different tissue interactions, important for hair growth and attachment.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

Curcuma aeruginosa extract combined with minoxidil effectively treats male-pattern baldness.