Familial forms of nephrotic syndrome

Which is the most frequent mode of inheritance of familial NS?

a. AD
b. AR
c. X-linked dominant
d. All

Genes involved in NS code most frequently for proteins of:

a. Glomerular basement membrane
b. Podocytes
c. Tubular epithelia
d. Mesangial cells

TRCP6 mutations are associated with congenital NS:

a. Yes, always
b. Often
c. Not yet
d. With Finnish nephropathy

PLCE1 usually causes DMS:

a. In most cases
b. The association has never been reported
c. Is more frequently associated with FSGS
d. Is usually associated with hermaphroditism

NPHS1 truncating mutation (Finmajor) is prevalent in:

a. Southern Europe
b. France
c. Finland
d. Only in Asia

Denys-Drash Syndrome is allelic with:

a. Frasier syndrome
b. Leigh syndrome
c. NPHS1
d. NPHS2

Which is the gene for Familial Steroid Sensitive NS?

a. LAMB2
b. ACTN4
c. WT1
d. Never reported

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