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Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Using animal names for skin conditions helps with learning and memory.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

COX-2 and Bcl-2 proteins are involved in Lichen Planus.

Laser-assisted drug delivery has shown improved treatment outcomes for skin conditions and has potential to reduce side effects and treatment time.

Oral valganciclovir improved a patient's skin condition caused by immunosuppression.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Men with certain types of baldness at age 45 may have a higher risk of colon cancer and colorectal adenoma.

Horse skin diseases are complex to manage and often require a biopsy for accurate diagnosis and treatment.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

Pannexin 3 is important for bone formation and the development of bone cells.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

New melanoma treatments can cause skin side effects, including skin cancer and rashes, but combining treatments may reduce these risks.

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.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

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.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

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.

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.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

COVID-19 may lead to severe skin necrosis without clear underlying causes, as seen in a diabetic patient who required leg amputation.