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The document discusses challenges in eye care, including treating melanoma before macular hole repair, bloody tears resolved by blood pressure control, eyelash regrowth in hair-pulling disorder with medication, a non-invasive method to detect eyelash mites, and the psychological factors affecting contact lens comfort.

Men with androgenetic alopecia may have more severe dry eye and meibomian gland dysfunction.

Cats and dogs with dermatophytosis show skin issues, with dogs having more severe symptoms.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The Hotz-Celsus surgery successfully fixed inward-turning eyelids in cattle.

Sheep with chronic Sarcoptes scabiei dermatitis have altered keratin expression in their skin.

Hair follicle stem cells can become corneal-like cells with the right environment.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The model can effectively help diagnose meibomian gland dysfunction automatically.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Finasteride, often used for hair loss, can potentially cause cataracts.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

New mutations in the DSG4 gene cause a rare hair condition.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Hair follicle stem cells can help treat eye surface issues by becoming corneal cells.

Treating cystoid macular oedema in uveitis is difficult and risky.

A baby with KID syndrome died from infections and organ failure at 18 months old.

A specific gene mutation causes severe skin and nail issues and hair loss.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Brodalumab is more effective than ustekinumab in treating psoriasis.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.