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The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

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

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

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

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Gene regulation could revolutionize hair color by altering pigmentation from within.

Hairless gene not strongly linked to baldness.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Herbal treatments can help with hair problems, but more research is needed.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

New treatments and diagnostic methods for various animal skin conditions showed promising results.