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A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Heavy metals like arsenic, cadmium, and lead can increase cancer risk and worsen outcomes.

Baby teeth stem cells can potentially grow organs and treat diseases.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

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

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The document explains the genetic causes and characteristics of inherited hair disorders.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Children with autoimmune gastritis showed improved intestinal health over time and should be checked for other autoimmune conditions.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

MOF controls skin development by regulating genes for mitochondria and cilia.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Mutant mice help researchers understand hair growth and related genetic factors.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

COX2 and ATP synthase control the size of hedgehog spines.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.