Search

everythinglearnresearchcommunity

for

Search:↓

Methotrexate effectively controls eye inflammation in Japanese patients with non-infectious uveitis but requires careful monitoring for side effects.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Jarilla-Coffea extract gel effectively and safely increases eyelash and eyebrow thickness in women.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

No single treatment is clearly effective for central serous chorioretinopathy.

Fusidic acid can be an effective topical treatment for superficial bacterial infections in dogs.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Cord blood platelets may have promising future medical uses but need more research.

ECCL should be considered in patients with specific skin and eye lesions.

Parry Romberg syndrome requires awareness and teamwork in primary care for proper diagnosis and management.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

A young woman developed a vision-threatening eye condition after using minoxidil for hair loss, which improved when she stopped the medication.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

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

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.

Treating cystoid macular oedema in uveitis is difficult and risky.

New treatments for relapsing multiple sclerosis are more effective and convenient but have higher risks of serious side effects.

SJS/TEN survivors often have severe, overlooked long-term physical problems that are not properly treated after leaving the hospital.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Low doses of some substances can be beneficial, while high doses can be harmful or toxic.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

The cosmetic industry should adapt to the varied beauty standards of ethnic groups and offer specialized treatments.

Wounds on the face usually heal with scars, but understanding how some wounds heal without scars could lead to better treatments.

Gefitinib can cause skin problems, diarrhea, and nausea, but rarely causes severe lung disease or hair loss.

The study aims to find the best treatment for central serous chorioretinopathy by comparing various options.

Some people with severe, long-lasting baldness responded well to a specific combination treatment.