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Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

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

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

Both tissue expansion and serial excision are effective for scar revision in the head and neck area.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

Covers common skin issues in kids, their diagnosis, treatment, and need for specialist care.

Micrografts are useful for healing wounds, regenerating bone and periodontal tissues, and improving hair transplantation outcomes.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

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

New treatments targeting specific genes show promise for treating keratin disorders.

A child had a rare case of scarring hair loss with skin disease, which is hard to treat and stressful.

Eating disorders can cause various hair problems, and while hair loss in these disorders is linked to metabolic syndrome, treatment focuses on specific medications and lifestyle changes for the syndrome.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

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.

Taking Propecia might lead to the development of cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

The regenerative solution, tSVF, is a safe and effective treatment for various conditions like aged skin, scars, wounds, and more, but more research is needed to find the best way to use it.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

Common skin conditions can greatly affect a person's mental health and social life.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.