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Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

The document concludes that proper diagnosis and combined treatments are key for hirsutism management, and weight loss may help overweight patients.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

The document concludes that early diagnosis and treatment of PCOS in teenagers is important for managing symptoms and preventing long-term health problems.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Gene linked to common hair loss found, may lead to new treatments.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Zinc can help with some skin problems, but its effectiveness varies depending on the condition.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Certain diets can affect skin conditions, but more research is needed to understand these relationships fully.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

Early diagnosis and aggressive treatment are crucial for Cicatricial Alopecia, and treatment effectiveness varies among patients.

Most patients with hair loss sought treatment for cosmetic reasons, were unhappy about their appearance, and had a family history of the condition, suggesting it may be inherited.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Massaging the scalp with a cosmetic containing certain natural inhibitors can significantly regrow hair in men with pattern baldness.

Hair restoration surgery has improved to transplant hair in natural groupings, but it's labor-intensive and can't fully restore normal hair density.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.