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The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

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

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Certain drugs that block specific enzymes can help treat prostate diseases.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Allopregnanolone changes gene expression in glioblastoma cells.

Reversing female hair loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

No link found between new male baldness genes and female hair loss.

Vitamin D and estrogen may help protect heart and kidney health, and maintaining sufficient vitamin D levels could be especially beneficial for African Americans, postmenopausal women, and people with chronic kidney disease.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

A gene called HDAC9 might be a new factor in male-pattern baldness.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The study found nine new hair protein genes in human hair follicles.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.