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Frontal fibrosing alopecia is a hair loss condition in postmenopausal women, similar to lichen planopilaris, with ineffective treatments.

Middle-aged women with chronic telogen effluvium experience increased hair shedding but usually don't get significantly thinner hair.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Some postmenopausal women with frontal fibrosing alopecia stopped losing hair with finasteride treatment, hinting at a possible hormonal cause.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The study found that Frontal Fibrosing Alopecia affects a broader age range of women and early treatment can help stop hair loss.

No effective treatment for frontal fibrosing alopecia was found, but oral 5-alpha-reductase inhibitors had the best response; for lichen planopilaris, topical corticosteroids were commonly used but had a high relapse rate.

Dutasteride may help stabilize Frontal Fibrosing Alopecia, but more research is needed.

A premenopausal woman had hair loss and skin issues, treated with topical steroids.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Chronic Telogen Effluvium is a hair loss condition in middle-aged women that usually doesn't lead to complete baldness.

Vitiligo causes white skin patches and is linked to autoimmune issues.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Hair transplantation may not work for Frontal Fibrosing Alopecia as transplanted hair was lost when the disease came back.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Trichoscopy helps diagnose and assess the severity of Frontal Fibrosing Alopecia.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Mutations in the KRT85 gene cause hair and nail problems.

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

Oral minoxidil shows promise in treating monilethrix-related hair loss.

Different factors help diagnose and treat hair loss accurately.

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

Mice with CBS deficiency are healthier on a low-methionine diet.

Herbal alternatives like saw palmetto and green tea may offer safe, effective treatment for hormonal hair loss.

Male pattern baldness affects 38.52% of Asian men in Bangkok, increasing with age and influenced by genes and environment.

Combination therapy with steroids and pimecrolimus improved or stabilized hair loss in most patients with Frontal Fibrosing Alopecia, who also had a high rate of hypothyroidism.

Caucasian hair is denser, but Asian hair is thicker in female pattern hair loss patients.