Michael Bromberg, MD, PhD, talks with Physician’s Weekly about renal disease in patients with paroxysmal nocturnal ...

FA is found to be more prevalent in populations, including South Africans, sub-Saharan Africans, Spanish Gitanos, US Ashkenazi Jews, and Europeans, due to inherited genetic mutations. In India, FA ...

Patients in the EU with Fanconi anaemia (FA ... FA is an inherited syndrome that impairs the body’s chromosomal repair systems, causing bone marrow failure, and leads to congenital malformations ...

More than half, or 67 percent, were women. Many patients had symptoms and test results suggesting Fanconi syndrome, a condition caused by damage to the renal tubules in the kidneys. Nearly 20 ...

Fanconi anemia (FA) is a rare genetic disorder ... and outcomes for children with FA in India. FA is a multi-system disease, requiring a comprehensive and interdisciplinary approach to clinical ...

In most cases, glycosuria develops because of high blood sugar or diabetes, symptoms may include: While less common, Fanconi ...

According to the Japanese Society of Nephrology, many people who fell ill after ingesting Kobayashi Pharmaceutical’s benikoji supplements are suspected of having developed Fanconi syndrome ...

Renal tubular toxicity including Fanconi Syndrome. Obtain baseline serum ferritin level, monitor monthly and adjust dose accordingly. Measure serum creatinine in duplicate before starting therapy ...