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Keratosis pilaris is common in young females, and dermoscopy helps diagnose it accurately.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Recognizing both trichostasis spinulosa and eruptive vellus hair cysts together is crucial for accurate diagnosis and treatment.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

New genetic mutations causing hair loss were found in a Chinese family.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

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

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

A girl inherited excessive body hair from her mother and grandmother.

Tph cells are linked to the severity of systemic lupus erythematosus.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Targeting THY1 can improve skin repair and healing.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

PC-associated alopecia has unique microscopic features.

Consider THPP in patients with muscle weakness and low potassium, as it is often underdiagnosed.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.