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A woman had meningitis caused by mixed connective tissue disease, not an infection.

Alopecia areata and polymyalgia rheumatica may be linked autoimmune conditions.

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

No clear link between specific gene and hair loss in Mexican brothers.

Two gene areas linked to male pattern baldness found, more research needed.

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

Using 5-alpha-reductase inhibitors, drugs for prostate issues and hair loss, may lead to eye abnormalities in men.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Hispanic/Latinx patients with alopecia areata often have it before age 40, with females and certain health conditions like rheumatoid arthritis more commonly affected.

CAG repeat numbers in the AR gene likely don't affect hair loss in Korean men.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Hair loss links to high blood pressure, high fat levels, and metabolic issues, suggesting early heart disease screening.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Aggressive immunosuppressive treatment improved a woman's severe heart condition linked to autoimmune disease.

Women under 55 with hair loss (AGA) may have a higher risk of heart disease (CAD).

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Tranexamic acid effectively reduced swelling episodes in a girl with a rare form of hereditary angioneurotic edema.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Severe hair loss (androgenetic alopecia) is linked to higher risk of heart disease (cardiovascular atherosclerosis).

A 65-year-old man with sudden abdominal pain and seizures was diagnosed with a rare, non-traumatic splenic rupture and treated without surgery.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.