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Flutamide and finasteride reduced sex hormones in pregnant hyenas, but increased them in males.

Digital games are part of new media but need a deeper look at their complex nature and cultural roots.

Foams improve drug absorption and release in various medical applications.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A 16-year-old girl with a hair-eating disorder needed surgery to remove a hairball from her stomach and small bowel.

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

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

The research identified new skin traits in mice, some linked to human skin conditions.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Researchers created a new mouse model for studying scleroderma.

Mutations in the KRT85 gene cause hair and nail problems.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A specific gene mutation causes severe skin and nail issues and hair loss.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.