Search

everythinglearnresearchcommunity

for

Search:↓

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.

Connective tissue nevi have distinct features, and reflectance confocal microscopy is useful for early diagnosis.

Epithelial elements in superficial angiomyxomas are non-neoplastic growths mimicking embryogenesis.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

Desmosomal adhesion is essential for healthy skin structure and function.

A new tool accurately identifies human cornea cell states and key factors.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Meibomian glands are like hair follicles without a hair shaft.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Benign follicular mucinosis involves immune cells attacking hair follicles.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

Using a perfusion system and 3D spheroid culture improves the growth of corneal cell layers for tissue engineering.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

CDH3-related disease causes worsening eye and hair issues.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

An isolated episcleral plasmacytoma can mimic episcleritis, making diagnosis challenging.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A 5-year-old boy has Nevus Comedonicus Syndrome, causing skin lesions and a cataract.

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.