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Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

The document concludes that correct diagnosis of alopecia types is crucial, scalp biopsies are important, and more research is needed.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Detailed patient history and physical exams are crucial for diagnosing hair loss.

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.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

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

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Bioactive molecules show promise for improving skin repair and regeneration by overcoming current challenges with further research.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Researchers found a gene mutation responsible for a rare hair loss condition.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

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.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Different combinations of human hair keratins affect how hair fibers form.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

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

Nail stem cells and Wnt signaling are important for fingertip regeneration but not sufficient for regenerating more complex limb structures.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Disrupted sleep patterns can harm skin and hair cell renewal, but melatonin might help.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

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.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

LLLT helps treat hair loss by increasing blood flow, reducing inflammation, and stimulating growth factors.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.