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Non-scarring alopecia in females affects emotional well-being and requires accurate diagnosis and personalized treatment.

Imiquimod can cause rare skin side effects, some irreversible, and long-term follow-up is important for users.

Too much male hormone in mothers can negatively affect the sexual behavior of both male and female baby mice.

The document concludes that different types of permanent hair loss conditions are related and early treatment is key to preventing further damage.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

The method can effectively extract biomedical information without needing expert annotation, performing better than previous models.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

The bulletin provides guidelines for diagnosing and managing PCOS, suggesting weight loss, hormonal contraceptives, and diabetes screening, with clomiphene for infertility and various treatments for excess hair.

Women with PCOS often have more belly fat and higher insulin levels, but belly fat isn't the only cause of their insulin resistance.

Estrogen Receptor ß (ERß) is the main hormone controller in human skin and hair follicles, not Estrogen Receptor α (ERα) or the Androgen Receptor (AR).

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

Hirsutism is a strong sign of high male hormones and metabolic problems in women with PCOS, but acne and hair loss are not.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Hormones, nutrition, and seasonal changes regulate hair growth cycles, with androgens extending growth phases and factors like aging and malnutrition affecting hair loss and thinning.

Men with common hair loss may have a higher risk of heart disease and diabetes, and should be checked for these conditions.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.