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An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

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.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

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 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.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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 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.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

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

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

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

Regulatory T-cells are important for healing and regenerating tissues in various organs by controlling immune responses and aiding stem cells.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

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

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

Short anagen syndrome involves a hair growth phase lasting 1.5 years.