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A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Laser hair reduction can sometimes cause a rare skin condition called Fox-Fordyce disease.

Recognizing and fully removing giant pilomatrixomas is crucial to prevent them from becoming cancerous.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

Children with marasmus have more resting hair follicles and thinner, less pigmented hair, showing long-term malnutrition.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Skin problems can indicate different diseases inside the body.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

A young woman with skin issues and weight loss improved after treating her pancreatitis and using skin treatments.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

PRP injections for hair loss may cause scalp nodules that can persist but often regress on their own.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Lichen planopilaris in men often involves scalp redness and itching, with some also having hair loss, mucosal lichen planus, or thyroid disease, and treatment improved symptoms in nearly half of the cases.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

The woman has Discoid Lupus Erythematosus and needs specialist care.

A kidney transplant patient developed pink skin bumps with spiny centers on her face and limbs.

Nevus comedonicus can appear later in life and affect both eyelids.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

Early diagnosis of Keratosis pilaris atrophicans faciei can lead to better, personalized treatments.

Mycophenolate mofetil may improve symptoms and stop hair loss in Lichen planopilaris, but more research is needed.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Severe hypothyroidism can cause unusual skin problems that improve with thyroid treatment.