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Finasteride in male rats causes liver and metabolic issues in their offspring.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A gene mutation causes woolly hair in a Syrian patient.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Woolly hair is a rare genetic condition with no effective treatments.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Passiflora incarnata may help with anxiety but has risks and drug interactions. There's a genetic link between Fragile X Syndrome and Autism Spectrum Disorder. 6.7% of urine cultures showed hospital-acquired urinary tract infections. Children used screens more during COVID-19, causing various health complaints. Autism Spectrum Disorder is often underdiagnosed in females. Dissociative disorders in childhood sexual abuse victims are more common in males. Most pregnant teenagers are not dissatisfied with their body image but worry about weight. Diagnosing tuberculosis after knee surgery is challenging due to non-specific symptoms. Post-COVID-19 syndrome is more common in older, severely affected patients. Psychiatrists should be part of pain management teams due to the psychological aspects of pain.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

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

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Hair loss in cancer patients can be related to the cancer itself, treatment, or other conditions, and understanding it is important for diagnosis and patient care.

Hair loss risk is influenced by multiple genes.