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Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

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.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

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 TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Hair loss gene found on chromosome 3q26.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

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

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

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

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.