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Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

Nail disorders are often related to jobs like housework and manual labor, with cosmetic issues being the main concern, and are commonly caused by skin diseases like psoriasis.

Doctors should consider psychological factors when treating skin conditions and work with mental health experts.

Mutations in keratin genes cause cell fragility and various skin disorders.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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.

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

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

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

Dermatological conditions are complex and treatments often have mixed results.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

The skin is a complex barrier that protects the body, regulates temperature, and helps with immune responses.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Found new possible treatments for hair loss.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

Nails can reveal important health information about skin and body conditions.

The document concludes that the girl's hairlessness is likely inherited from her parents.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.