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MCHR2 gene duplications may be linked to alopecia areata.

Effective sleep apnea treatment may reverse cognitive decline in Alzheimer's.

The woman was diagnosed with systemic lupus erythematosus (SLE) after initial misdiagnosis and improved with proper treatment.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

Most patients with cutaneous lupus erythematosus in Bangladesh are young women, with chronic forms and photosensitivity being common.

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

Upadacitinib effectively treated severe atopic dermatitis, vitiligo, and alopecia areata in one patient.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The document concludes that using gadolinium-based contrast agents during MRI can be linked to Nephrogenic Systemic Fibrosis in patients with severe kidney disease.

A JAK inhibitor improved both severe hair loss and chronic skin disease in one patient.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Surgical removal is advised for large congenital blue nevi due to rare cancer risk.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Upadacitinib effectively treats pyoderma gangrenosum.

A rare scalp disease causes hair loss, pus-filled nodules, and scarring.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.