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Linear cutaneous lupus erythematosus on the scalp is rare, often affects young Asians, and can be treated with specific medications.

ROR-alpha may increase the growth of certain breast cancer cells by boosting aromatase, which could affect breast cancer prognosis.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

Trichoblastoma in the breast can be mistaken for cancer, so expert review is crucial to avoid misdiagnosis.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

A woman with lupus had rare severe symptoms but improved with treatment.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Some hair products can create false signs on scalp examinations, leading to wrong diagnoses.

5-ARI therapy may help prevent prostate cancer progression.

A patient's skin rash did not affect the area where a previous viral rash was healing, suggesting a rare immune response.

A girl had rickets due to a gene mutation affecting vitamin D response.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Persistent ED in Propecia users is not due to abnormal blood flow.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

Brunsting-Perry pemphigoid can cause scarring hair loss and may be underdiagnosed.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Anifrolumab significantly improved skin lesions and hair regrowth in severe discoid lupus.

A 14-year-old girl's black hair showed unique color changes, suggesting early greying.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

A 9-year-old boy had a rare scalp condition usually seen in young men.

Platelet-rich plasma therapy may rarely trigger herpes zoster ophthalmicus.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

Peripilar signs can help diagnose androgenetic alopecia and reveal its cause.