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The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

Neck burn scar contracture recurrence is more likely with larger neck defects, and closer follow-up can help detect it sooner.

A woman with Cushing's syndrome improved after surgery to remove a tumor causing the condition.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Traction may not be the only cause of cicatricial marginal alopecia.

Pincer nails are rare in lupus patients and may be managed conservatively.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Some burn patients grew extra hair in areas treated with pressure garments or silicone.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

Tofacitinib may cause nerve damage in the brain, so monitor for neurological symptoms.

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Trichotillomania treatment is improving with behavior therapy and new drug approaches, but challenges like stigma and underdiagnosis remain.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

People with telogen effluvium and scalp discomfort might have low vitamin B12 and could benefit from B12 supplements.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Early treatment of hair-pulling disorder is crucial to prevent permanent hair loss and scarring.

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

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

Cabergoline helped a boy with Cushing disease get better after surgery and radiotherapy didn't work.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.