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Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

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

People with Down's syndrome often have more skin problems due to a weak immune system.

Researchers created early-stage hair-like structures from skin cells, showing how these cells can self-organize, but more is needed for complete hair growth.

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

Use specific tools to measure quality of life in alopecia areata patients and improve future treatments.

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

NF-κB is crucial for different stages and types of hair growth in mice.

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

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.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

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

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

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.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

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.

The study concluded that hair loss in Indian women is not significantly linked to anemia or thyroid problems, but checking thyroid function could help those with ongoing hair loss.

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.

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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.