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Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

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.

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

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

Finasteride may help reduce tic severity in male Tourette syndrome patients.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Mice with alopecia areata had wider lymphatic vessels in their skin.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Mutations in the AR gene cause hair thinning and loss.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

Epimorphin, a protein, plays a key role in the development of hair follicles in human fetuses, but it doesn't help in maintaining the stem cell population of the follicular skin layer.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

VDR regulation varies by tissue and is crucial for its biological functions.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Hair follicle stem cells help maintain skin health and could improve skin replacement therapies.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Different processes create patterns in skin and things like hair and feathers.

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

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.