Search

everythinglearnresearchcommunity

for

Search:↓

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Carrying heavy loads harms donkeys' health, causing pain and injuries.

PRP therapy helps heal pediatric surgical wounds faster and with fewer scars but needs more research for safety and cost.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Modern society values both traditional beauty and imperfections, but media pressures lead to more cosmetic enhancements and ethical concerns.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Terbinafine is the most effective medicine for fungal nail infections, especially for diabetics and those with weak immune systems.

The model and estimator can predict drug exposure in kidney transplant patients well.

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

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

The document concludes that treating skin conditions should include psychological care and a multidisciplinary approach is essential for effective management.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Changes in gut bacteria can contribute to the development of Polycystic Ovary Syndrome (PCOS), affecting metabolism, immunity, and causing inflammation. Treatments may involve adjusting these factors.

Many displaced schoolchildren in Cameroon are malnourished, with high rates of thinness, stunting, underweight, and deficiencies in iron and protein.

Sostdc1 controls the size and number of hair and mammary gland structures.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

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

Experts advise using sunscreen and proper skin care before, during, and after procedures to speed healing, prevent complications, and reduce scarring.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

Bio-pulsed stimulation increases production of beneficial vesicles from bird stem cells that improve skin and hair cell functions.