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The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

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

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Esthetic surgery complications can include infections, nerve injury, and more; proper evaluation and technique help prevent them.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Treating H. pylori infection might help cure alopecia areata.

Hospital staff have a higher rate of hair loss than the general population.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Vertical sleeve gastrectomy improved metabolism, behavior, and reproduction in obese rats with PCOS.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

TNF-alpha inhibitors can cause various immune-related skin issues.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.

Skin diseases have a small to moderate impact on the quality of life of patients in Goa, India.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Bariatric surgery may help severely obese teenagers but has risks and requires careful patient selection and long-term care.

An enzyme other than TNAP might be responsible for vitamin B-6 metabolism in the skin.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

About 3% of high school girls aged 14-18 in Isfahan, Iran, have polycystic ovary syndrome.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Environmental factors, hormones, nutrition, and stress all significantly affect skin health and aging.

Researchers isolated a new type of stem cell from mouse skin that can renew itself and turn into multiple cell types.

5% minoxidil foam is a safe, effective treatment for male pattern hair loss, with increased hair count and few side effects.

Low vitamin D levels can significantly contribute to hair loss, especially in women aged 35-45. Correcting these levels early may help prevent and treat this condition.