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Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Accurate assessment of puberty using Tanner staging is crucial for identifying normal and abnormal development.

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.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

People with polycystic ovary syndrome may have a higher risk of heart problems due to abnormal nervous system control of their heart and blood pressure.

Blocking the HEDGEHOG-GLI1 pathway can reduce keloid growth and may be a potential treatment.

A Nigerian teenager was diagnosed with neuropsychiatric lupus, showing various severe symptoms and abnormal lab results.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Women with PCOS often have metabolic issues like insulin resistance and a higher risk of diabetes and abnormal lipid levels.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Combining traditional hair removal methods with modern technology could improve cosmetology.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

Vitamin supplements may not improve hair thickness or density in patients with non-scarring hair loss.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Traditional Korean medicine combined with modern technology may improve hair removal treatments.

Genetic hair disorders can indicate other hidden health problems.

Anabolic steroids may help prevent aging effects by reducing toxicity, not by their usual functions.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Cathepsin L is essential for normal hair growth and development.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

Polycystic ovary syndrome causes high male hormone levels, leading to symptoms like excess hair, acne, and fertility problems.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Higher resolution images are needed to identify scarring and fine hair in alopecia.

Two siblings have a rare genetic condition causing curly, coarse hair.

Mesalazine may help treat extensive alopecia areata effectively.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.