Search

everythinglearnresearchcommunity

for

Search:↓

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

A young woman had a rare scalp tumor usually found in older women.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Eosinophilic cystitis is often misdiagnosed, but accurate diagnosis and treatment improve outcomes.

Surgical treatment can significantly reduce or eliminate migraine symptoms.

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.

A rare eyelid tumor was successfully diagnosed and removed, highlighting the need for careful examination.

An 18-year-old boy had a harmless skin nodule near his nose with hair and oil glands inside.

A 47-year-old man's eyelid swelling didn't improve with basic treatments, so a biopsy was needed.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

A bladder rupture from prostate treatment was healed with catheterization and antibiotics.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

A 62-year-old woman got a lump on her eyelid from tiny mites, which is the first time this has happened.

A patient's rare benign tumor in the neck was removed successfully with proper function of the facial nerve maintained.

A man developed neurological issues from SARS-CoV-2 without severe breathing problems, worsening to death.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A 25-year-old Malay fireman had skin bumps on his neck that were removed successfully after other treatments failed.

Irradiating the whole central nervous system can lead to over 50% of patients with cerebellar medulloblastoma surviving three years.

Sertoliform endometrioid carcinoma of the ovary, though rare, has a good prognosis when treated early.

A rare skin growth in a baby was successfully removed without coming back.

A family medicine approach improves treatment and quality of life for children with enterobiosis.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Intralesional cidofovir might be a viable alternative treatment for certain conditions.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.