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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.

Children with trichotillomania often pull hair from their scalp, and parents may not notice; stress can trigger it, and asking detailed questions helps in diagnosis and treatment.

Post-finasteride syndrome causes lasting sexual, neurological, and physical side effects in some people after taking finasteride.

Testosterone therapy and surgeries like mastectomy improve transgender men's lives and mental health with low risks and high satisfaction.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

A woman showed neurological symptoms from psittacosis linked to bird exposure, improving after antibiotic treatment.

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

The document suggests a new model for evaluating public research that better captures the full value of knowledge creation and use, using PCOS research as an example.

Cross-sex hormone therapy is important for managing gender dysphoria and requires careful monitoring and healthcare provider education.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

In Japan, sex reassignment surgery for gender identity disorder faces challenges and needs better medical support and education.

The superficial temporal artery flap is a reliable method for reconstructing complex facial defects with minimal complications.

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

Most insurance companies do not cover extra gender-affirming surgeries, with coverage being low and inconsistent.

Cantú syndrome may be linked to pituitary adenomas.

Treating hair loss requires a comprehensive approach that addresses both physical and emotional aspects, with a focus on diagnosis, patient education, and good communication.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Combining mood stabilizers with antipsychotics is more effective for treating children with bipolar disorder than using mood stabilizers alone.

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

The document concludes that hormone therapy is essential for treating gender dysphoria, with specific drugs and monitoring protocols recommended for safety and effectiveness.

New signs like changes in blood markers, physical symptoms, and behavioral shifts may help detect hidden steroid use in athletes.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Megasessions in hair transplant can cover more area or increase density but need a skilled team and careful planning, and have both benefits like less downtime and risks like lower graft survival.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Facelifts can lead to high patient satisfaction and a quick recovery when done correctly.

The document concludes that individualized reconstruction plans are essential for improving function and appearance after head and neck burns.