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No single treatment is clearly effective for central serous chorioretinopathy.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

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.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

A 65-year-old man with sudden abdominal pain and seizures was diagnosed with a rare, non-traumatic splenic rupture and treated without surgery.

Acne keloidalis is a chronic skin condition on the back of the neck in young black men, needing surgery for severe cases.

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

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.

The skin lesion was diagnosed as a matrical cyst with unusual features.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

Stem cells in the cornea show unexpected flexibility and have important implications for medicine.

Most patients' skin darkening after sclerotherapy fades on its own within 6-24 months.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

Recognizing and treating oral lichen sclerosus is important, but treatment guidelines are lacking.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

A woman developed permanent hair loss after a face-lift surgery despite various treatments.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.