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The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

A gene mutation in mice causes permanent hair loss and skin issues.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Plant-based remedies may treat hair loss by reducing inflammation and improving insulin resistance.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A rare ear-area hair cyst was successfully removed from a 10-year-old boy.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Too much thymosin beta4 causes weird teeth and more hair growth in mice.

Excessive hair growth in women, often from high androgen levels, is usually caused by PCOS, and can be treated with hair removal, medication, and possibly weight loss.

Hormone treatment for transsexual individuals is effective but carries risks like thromboembolic events and mood changes, with most side effects being minor and reversible.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Female pattern hair loss is common, linked to polycystic ovarian syndrome, and treated with topical Minoxidil.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The research found that polycystic ovary syndrome (PCOS) has two distinct types, with one having more severe hormone and insulin issues.