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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Modified superoxide dismutase may trigger an autoimmune response in alopecia areata.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Antihepcidin antibodies may treat inflammation-induced anemia by improving iron metabolism.

A woman with severe hair loss due to systemic sclerosis regrew her hair in 4 months using a combination of treatments.

A rare biotin deficiency in an Iraqi family caused severe symptoms but was successfully treated with lifelong biotin.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

Sertoli cell transplants can reduce inflammation and improve sperm quality.

A special diet can fix hair problems in argininosuccinase deficiency.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

Peginterferon alpha-2a effectively treats acute hepatitis C in hemodialysed patients, despite some side effects.

Consider amyloidosis in patients with specific nail changes and check for systemic issues.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Ayurvedic medicine helped increase a young woman's hemoglobin levels and improved her anemia symptoms.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Selenium therapy improved health in cystic fibrosis patients with fewer side effects at a lower dose.

Age-related immune changes significantly affect disease development in other systems.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

WNT10A gene mutations cause short anagen hair syndrome.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Many people with inflammatory bowel disease have a vitamin C deficiency, which can lead to scurvy symptoms.