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Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

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

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Basal cell epithelioma-like changes are most similar to normal basal cells.

A baby girl's hair turned straight on one side due to a neck tumor and surgery, but it returned to curly as she recovered.

A man developed a unique rash on his neck after taking niacinamide, and doctors recommend considering niacinamide as a cause for similar rashes and using dermatoscopy for diagnosis.

The scalp has a natural speckled pattern of increased pigment around hair follicles, possibly linked to local hormone production.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Non-melanoma skin cancer in darker-skinned people can be misdiagnosed, so doctors need to be more aware to diagnose it correctly and early.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Keratinocyte cytokines and genetic variations influence the development of moles and skin pigmentation.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

The study suggests that acne keloidalis nuchae is linked to conditions like pseudofolliculitis barbae, scalp infections, metabolic syndrome, and is more common in males with an average onset age of 25.4 years.

A woman with a rare hair loss condition developed skin cancer in the bald area.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

Hair ages as the cuticle wears down, especially beyond 1 meter from the root, affecting its strength and shine.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

The platform effectively grows lung cancer cell spheroids for drug testing.

Environmental factors can greatly reduce drug levels in hair.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Men face more severe COVID-19 outcomes, while women are more likely to have long-term symptoms.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.