Vertaling van "familiair idiopathisch steroïdresistent nefrotisch syndroom " (Nederlands → Engels) :

familiair idiopathisch steroïdresistent nefrotisch syndroom
Nephrotic syndrome with often-early onset defined by severe proteinuria with low serum albumin and possible oedema. This disease is rare but severe as it usually progresses to end-stage renal failure. Mutations in the NPHS2 gene (chromosome 1q25-q31

sporadisch idiopathisch steroïdresistent nefrotisch syndroom
A heterogeneous entity. Its prevalence in the general population is unknown. Nephrotic syndrome has manifestations of marked proteinuria, with reduced plasmatic levels of albumin, and potentially with oedema. Familial forms are in most cases related

familair steroïdresistent nefrotisch syndroom met perceptief gehoorverlies
A rare genetic coenzyme Q10 deficiency with characteristics of sensorineural deafness and severe progressive nephrotic syndrome not responding to steroid treatment. Clinical manifestations include early onset proteinuria, hypoalbuminaemia and oedema,