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Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Using steroids can increase the risk of heart problems.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Use finasteride, dutasteride, and minoxidil for hair loss treatment.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Minoxidil effectively treats female pattern hair loss.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Skin side effects from EGFR inhibitor cancer treatment can be managed effectively, often without stopping the medication.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Doctors have known about fungal skin infections for a long time, but only made major progress in understanding and treating them since the mid-1800s.

Fungal infections in lab animals can interfere with research.

Mutations in certain receptors can cause diseases and offer new treatment options.

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.

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

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Merkel cells may have roles in sensing magnetic fields, creating fingerprints, Reiki energy healing, passing on environmental information to offspring, and influencing hair shape.

Aminopterin was somewhat effective in acute lymphoblastic leukemia in children but did not increase survival time.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.