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Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

Early detection and stopping the drug are key to managing DRESS, and careful monitoring is important due to possible severe reactions.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

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

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

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.

Some treatments work for common baldness, but there's less evidence for other hair loss types, and more research is needed.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Early onset hair loss linked to genetics and androgen levels.

Type I interferons play a key role in the development of various skin diseases.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

People with Seasonal Affective Disorder have different brain activity in certain areas when resting.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

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.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Meis1 is crucial for skin health and tumor development.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.