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The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

A girl with Evans' syndrome had her low platelet count successfully treated with zanubrutinib.

Microneedling is a simple, affordable treatment that helps with scars, wrinkles, stretch marks, and hair growth by boosting collagen.

Genetic testing is crucial for diagnosing rare hair loss disorders.

MK-2206 was safe and effectively blocked AKT signaling in cancer patients, warranting more trials.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Hydroxychloroquine and chloroquine are not recommended for COVID-19 treatment due to insufficient evidence and safety concerns.

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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

CDH3-related disease causes worsening eye and hair issues.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Using 5-alpha-reductase inhibitors, drugs for prostate issues and hair loss, may lead to eye abnormalities in men.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

Using a diode laser for hair removal without eye protection can cause serious eye injuries.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Treating cystoid macular oedema in uveitis is difficult and risky.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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

A new genetic mutation was found causing hair and eye issues in a boy.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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

Men taking dutasteride may have a higher risk of age-related macular degeneration.

Hair loss might be linked to eye aging due to inflammation markers in blood.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.