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An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Acne keloidalis nuchae is a hair loss condition affecting men of African descent, causing scar-like bumps on the scalp and neck.

Blocking Oncostatin M's role in the JAK-STAT pathway can stimulate hair growth in mice.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Chemotherapy and certain hair care practices can cause severe hair matting.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Pemphigus vulgaris involves specific immune cells and B cells that produce antibodies causing skin blisters.

The pony's skin condition improved significantly with prednisolone treatment.

A rare skin condition was identified and planned for treatment in an elderly man.

Localized hair growth and fat loss may share a common cause in lupus panniculitis.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Baricitinib may help treat frontal fibrosing alopecia and facial papules.

Cicatricial alopecia can progress to complete hair loss, making diagnosis and management difficult.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

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

Hair loss in Lichen Planopilaris is caused by immune system issues damaging hair follicles and stem cells.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

Most patients with Lichen planopilaris improved with acitretin, but treatments often didn't work well; preventing infection in skin surgery is important, and bupivacaine might be a better anesthetic.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The document concludes that molluscum contagiosum is a common, benign skin infection in children, often healing without scarring.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Recognizing and treating oral lichen sclerosus is important, but treatment guidelines are lacking.

Razor bumps are linked to a genetic variant, misoprostol helps erythromelalgia pain, steroid ointments don't affect skin rhythms, and certain antibodies are common in localized scleroderma.

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

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Oral minoxidil may help improve fragile hair.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.