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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.

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

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

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

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

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

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

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

Cancer treatments targeting specific cells often cause skin, hair, and nail problems, affecting patients' lives and requiring careful management.

Nitroxide drugs can safely and effectively treat age-related diseases like macular degeneration and cardiovascular issues.

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Neurotoxins can affect neurotransmitter release and have potential in treating muscle, pain, and cancer conditions, but more research is needed on how they work.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Miz1 is essential for proper hair structure and growth.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

People with severe hair loss have lower zinc levels in their blood.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Adult hair follicle cells can create new hair follicles from corneal cells with the right support.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

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

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.