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The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

NG2 is crucial for normal skin and hair development in mice.

Improve skin paddle appearance after head and neck reconstruction using tissue expansion, rearrangement, and flaps.

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

Using cidofovir cream for a rare skin disease can cause skin darkening.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

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

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

The neck mass was a rare benign "wattle," surgically removed for diagnosis and appearance.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

A 25-year-old man had an unusual case of benign skin tumors and hair loss.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

A protocol was developed to create 3D skin models from adult diseased cells to study Small Fiber Neuropathy.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

A rare case of hair loss was linked to breast cancer spreading to the scalp, but treatment was effective.

Tinea faciei should be considered in neonatal vesicular lesions and confirmed with KOH examination and culture.

Recognizing trichofolliculomas is important to avoid unnecessary surgery.

Trichoblastic carcinoma may be a distinct type of skin cancer different from basal cell carcinoma.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Nail disorders not caused by infection are common and can look similar, with psoriasis being the most frequent and having specific nail symptoms.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Epithelial elements in superficial angiomyxomas are non-neoplastic growths mimicking embryogenesis.

Keratoacanthoma and some squamous cell carcinomas are linked to hair follicles, while others are not.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.