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Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

The substances improved hair regrowth and protected hair cells in humans and mice.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Early detection and treatment of hair-thread tourniquet syndrome in young girls is important to prevent serious harm.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

The document covers all aspects of plastic and reconstructive surgery, from basic techniques to specific procedures for various body parts.

Different species use the same genes for tooth regeneration.

The 2023 guideline for PCOS suggests using updated diagnostic criteria, assessing related health risks, and recommends lifestyle changes and specific treatments for symptoms and fertility issues.

The 2023 guideline advises a detailed approach for PCOS, focusing on early detection, lifestyle and medical treatments, and managing health risks.

Eyelid cells share signaling components but differ in pathway activity.

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.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

5% Azelaic acid is as effective as 2% Minoxidil for female pattern hair loss and could be an alternative for those allergic to Minoxidil or pregnant.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

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

K16 can partially replace K14 but causes hair loss and skin issues.

The most common skin problems in Indian children are infections and eczemas.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Lipedematous scalp is mainly caused by an increase in fat tissue under the skin and is different from lipedematous alopecia.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

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

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.