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Surgery on a baby with a skin disorder improved eyelid position and eye health.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

New genetic mutations linked to rare skin disorders were found in three newborns.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Newborns' hair shows how much caffeine their mothers drank during pregnancy.

The document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

Hair elemental analysis could be useful for health and exposure assessment but requires more standardization and research.

Researchers found over 40 compounds in Bituminaria bituminosa, including many flavonoids and some with potential for medical and hair care uses.

Herbal nano-formulations show potential for effective skin delivery but need more research.

Hair color and length affect metabolite profiles in hair, so they should be considered in hair analysis.

The document lists various dermatology topics, treatments, and diagnostic methods.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Papain and bisulfite break down human hair by dissolving parts of it.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Fresh plasma transfusions did not help treat Leiner disease in an infant.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Different combinations of human hair keratins affect how hair fibers form.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.