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The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Treatment with methotrexate and prednisolone led to complete hair regrowth and no relapse for 2 years.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

Infants with scalp injuries developed a skin condition that improved with steroid creams.

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

Women with PCOS have distinct retinal changes compared to healthy women.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

A rare skin condition caused scarring hair loss on the scalp.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Frontalis suspension surgery using autologous fascia lata is effective for treating unilateral congenital ptosis with poor levator function.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

A girl had two rare hair conditions that helped understand their overlap.

A woman with Sheehan syndrome improved with hormone treatment.

Skin issues are common in people with neurodegenerative diseases.

Soft-tissue calcification is rare in systemic lupus erythematosus.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

SLE can increase the risk of blood clots, leading to heart failure, but treatment can improve heart function.

Researchers found a new sign of fungal infection in some patients with Seborrheic Dermatitis.

SET7/9 enzyme affects cell growth and diseases like cancer, diabetes, and obesity.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.