Search

everythinglearnresearchcommunity

for

Search:↓

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

Human hair follicle cells can be successfully transformed into different types of cells, but not more efficiently than other adult cells.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

Leptin helps start the growth phase of hair.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Skin-derived stem cells can become various cell types, including germ cell-like and oocyte-like cells.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Adding human blood vessel cells to hair follicle germs may improve hair growth and quality.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

The hepatitis B vaccine did not cause hair loss in the tested mice.

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.

Alopecia areata involves immune response and gene changes affecting hair loss.

Stress can worsen skin conditions and affect mental health, so doctors should include stress management in skin treatment.

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.

Researchers identified specific genes that are important for mouse skin cell development and healing.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

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

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

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

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

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

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.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.