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Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

Two newborns with rare skin infections were successfully treated with antifungal cream.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

A patient experienced permanent hair loss due to an allergic reaction to a corticosteroid injection.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Uveodermatological syndrome in dogs is hard to manage and can lead to blindness despite treatment.

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

A person with thyroid problems had rare, swollen, bald spots on their scalp caused by a condition usually found on the shins.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

An 84-year-old man developed a rare scalp condition from a cancer drug but continued treatment as it was otherwise well tolerated.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Three dogs with a rare skin condition improved with treatment.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

JAK inhibitors show promise for treating various skin disorders effectively and safely.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

A rare benign skin nodule was found on the buttock, a unique location for this condition.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Doctors should consider SLE in males even if antinuclear antibody tests are negative.

Early treatment with corticosteroids and immunosuppressants is crucial for managing Vogt-Koyanagi-Harada disease.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.