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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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.

Researchers found a new mutation causing total hair loss from birth.

Hairless gene not strongly linked to baldness.

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.

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

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Taking Propecia might lead to the development of cataracts.

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.

Mutation in hairless gene may increase hair loss risk.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

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

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.

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.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

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

Mutation in hairless gene may increase hair loss risk.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

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

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

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

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

The HR protein's role as a repressor is essential for controlling hair growth.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.