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The meeting discussed medical findings, including benefits of certain treatments for cancer and heart conditions, and highlighted issues like poor adherence to preventive measures and skill gaps among interns.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Chemotherapy improved a girl's painful foot condition linked to pachyonychia congenita.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Using neurohormones to control keratin can lead to new skin disease treatments.

Hair color is influenced by genetics and can indicate certain health conditions.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

The review suggests limited treatments for common hair loss conditions, with potential for future improvements.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

A new mutation in the HR gene causes hair loss in a specific family.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

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.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Stopping certain drugs can improve skin conditions, arsenicosis affects over half of a Bangladeshi village, males are more vulnerable, and certain treatments are effective for warts, acne, and psoriasis. Smoking and drinking are linked to psoriasis in men, a cream helps with a type of skin cancer, and low iron levels don't directly cause chronic hair loss in women.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

A new gene variant in the DSP gene is linked to a unique type of hair loss.