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Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

The document concludes that doctors should carefully consider off-label drug use in dermatology and always inform patients, while more research is needed on the safety and effectiveness of such practices.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

Murine hair has specific types of ceramides and glucosylceramides but lacks acylceramides.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.

Thermal spring waters and their microbes could be good for skin health and treating some skin conditions in skincare products.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

European dermatologic treatments focus on lifestyle and psychosocial factors, use diverse methods like baths and climate therapy, and emphasize the importance of diet and supplements for skin health.

An adult with a rare skin condition improved with tazarotene treatment.

New genetic discoveries may lead to better treatments for alopecia areata.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Newborns with ichthyosis need specific care based on their skin type.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

The four patients have a unique type of ichthyosis affecting hair follicles.

Balneophototherapy effectively treats ichthyosis linearis circumflexa but may need ongoing treatment due to short remission.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

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

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

A woman's skin and hair conditions improved after her cancerous tumor was removed.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Removing a tumor may resolve associated skin and hair symptoms.

A new gene mutation linked to a skin condition was found in a Spanish family.