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Most hair loss disorders can be accurately diagnosed and treated in an outpatient setting.

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.

Substance from human umbilical cord blood cells promotes hair growth.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

Canine epidermal neural crest stem cells could be a promising treatment for spinal cord injuries in dogs.

Two-photon microscopy effectively tracks live stem cell activity in mouse skin with minimal harm and clear images.

Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.

Vitamin D and calcium are important for quick and effective skin wound healing.

Ethanamizuril is safe for rats at 20 mg/kg feed, but higher doses cause hair loss, organ changes, and liver, kidney, and lung damage.

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.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The AC 2 peptide from Trapa japonica fruit helps protect hair cells and may treat hair loss.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

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.

CD61 is important for mouse tooth cell growth and works through Lgr5.

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

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Dermal EZH2 controls skin cell development and hair growth in mice.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

The document explains how to create detailed biological pathways using genomic data and tools, with examples of hair and breast development.

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.

Iron deficiency might contribute to hair loss in women.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.