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AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

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.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Spironolactone may help reduce hair loss in androgenic alopecia.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Hair loss can significantly affect a person's self-esteem and body image, especially in young people, those who value their looks highly, and women.

Platelet-rich plasma, taken from a person's own blood, can help rejuvenate skin, stimulate hair growth, and treat hair loss, but more research is needed to confirm its safety and effectiveness.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

EGFR inhibitors can cause various skin issues during cancer treatment, and managing these is important for patient care.

The article concludes that dermatologists should prescribe lifestyle drugs carefully and consider mental health treatments for patients with disorders like BDD.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

Gambogic Amide helps maintain hair color and promotes hair growth.

ILC1 cells contribute to hair loss in alopecia areata.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Dermatologists often neglect hair disorders due to complexity and lack of clear treatments, impacting patient care and highlighting the need for better education and interest in this area.

New treatments targeting specific genes show promise for treating keratin disorders.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

FOXN1 gene variants cause low T cells and immune issues from birth.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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.

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.

Runners often face skin problems like blisters and infections, and both prevention and early treatment are important.

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.

HOXC13 is essential for hair and nail development by regulating Foxn1.