TY - JOUR
T1 - Renal function in angiotensinogen gene-mutated renal tubular dysgenesis with glomerular cysts
AU - Hibino, Satoshi
AU - Sasaki, Hiroshi
AU - Abe, Yoshifusa
AU - Hojo, Akira
AU - Uematsu, Mitsugu
AU - Sekine, Takashi
AU - Itabashi, Kazuo
N1 - Publisher Copyright:
© 2014, IPNA.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Background: Inherited renal tubular dysgenesis (RTD) is caused by mutations in the genes encoding the components of the renin–angiotensin system (RAS). RTD is characterized by oligohydramnios, renal failure, neonatal hypocalvaria, and severe hypotension. The histological characteristics, underlying mechanism, and long-term prognosis remain poorly known. Case-diagnosis/treatment: We describe here a 4-year-old female with RTD. Endocrinologic analysis showed a discrepancy between low plasma renin activity and high active renin concentration, suggesting a loss of the renin substrate, angiotensinogen (AGT). Direct sequencing revealed a frameshift deletion at nucleotide 1,355 in exon 5 in the AGT gene. Although a histological hallmark is regarded to be the absence or poor development of the proximal tubule, the patient does have minimally impaired function of the proximal tubule. Glomerular cysts without glomerular tufts were noted in approximately half of the glomeruli. The urinary concentrating ability and sodium reabsorption and potassium excretion in the distal nephron were severely affected. Conclusions: The patient has an impaired function of the distal nephron despite minimally affected function of the proximal tubule, probably attributed to renal tubular dysgenesis and fetal hypoperfusion. The renal tubular maturity and the severity of ischemic injury may be key determinants of the clinical symptoms and pathological findings in RTD, in which the RAS plays an important role.
AB - Background: Inherited renal tubular dysgenesis (RTD) is caused by mutations in the genes encoding the components of the renin–angiotensin system (RAS). RTD is characterized by oligohydramnios, renal failure, neonatal hypocalvaria, and severe hypotension. The histological characteristics, underlying mechanism, and long-term prognosis remain poorly known. Case-diagnosis/treatment: We describe here a 4-year-old female with RTD. Endocrinologic analysis showed a discrepancy between low plasma renin activity and high active renin concentration, suggesting a loss of the renin substrate, angiotensinogen (AGT). Direct sequencing revealed a frameshift deletion at nucleotide 1,355 in exon 5 in the AGT gene. Although a histological hallmark is regarded to be the absence or poor development of the proximal tubule, the patient does have minimally impaired function of the proximal tubule. Glomerular cysts without glomerular tufts were noted in approximately half of the glomeruli. The urinary concentrating ability and sodium reabsorption and potassium excretion in the distal nephron were severely affected. Conclusions: The patient has an impaired function of the distal nephron despite minimally affected function of the proximal tubule, probably attributed to renal tubular dysgenesis and fetal hypoperfusion. The renal tubular maturity and the severity of ischemic injury may be key determinants of the clinical symptoms and pathological findings in RTD, in which the RAS plays an important role.
KW - Angiotensinogen
KW - Glomerular cysts
KW - Nephrogenic diabetes insipidus
KW - Renal tubular dysgenesis
KW - Rennin–angiotensin system
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U2 - 10.1007/s00467-014-3007-0
DO - 10.1007/s00467-014-3007-0
M3 - Article
C2 - 25414114
AN - SCOPUS:84941561826
VL - 30
SP - 357
EP - 360
JO - Pediatric Nephrology
JF - Pediatric Nephrology
SN - 0931-041X
IS - 2
ER -