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Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

A specific genetic deletion in goats affects cashmere yield and thickness.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

No significant link between male pattern baldness and COVID-19 severity was found.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

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.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

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

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

Betacoronaviruses, like COVID-19, may cause hormone system dysfunction and affect disease susceptibility and severity.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

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.