Zusammenfassung der Ressource
renal tubular disorders
- abnormalities of renal tubular
function occur @ any point
along length of nephron &
affect any of substances
handled by it
- generalised proximal tubular dysfun (Fanconi syn)
- prox tubule cells very metabolically active
- esp vulnerable to cellular damage
- cardinal features: urinary loss of
- amino
acids
- glucose
- phosphate
- bicarbonate
- Na+
- Ca2+
- K+
- urate
- causes
- idiopathic
- secondary to
inborn errors of
metabolism
- cystinosis
- autosomal
recessive disorder
causing intracellular
buildup of cystine
- glycogen storage disorders
- Lowe syn (oculocerebrorenal dystrophy)
- galactosaemia
- fructose intolerance
- tyrosinaemia
- Wilson disease
- acquired
- heavy
metals
- drugs & toxins
- vit
D
def
- consider in child presenting w/
- polydipsia & polyuria
- salt
depletion &
dehydration
- hyperchloraemic
metabolic acidosis
- rickets
- failure to thrive/poor growth
- specific disorders classifed accord to part of tubule affected
- proximal tubule
- glycosuria
- asymptomatic
- reduced
reabsorption
of glucose
- cystinuria
- reduced
reabsorption of
cystine & dibasic
amino acids
- renal
calculi
- vit D
resistant
rickets
- reduced reabsorption of phosphate
- rickets
- pseudohypoparathyroidism
- increased reabsorption of phosphate
- obesity
- depressed
nasal
bridge
- short
fingers
(2nd, 4th
& 5th)
- hyperuricosuria
- increased secretion or
reduced reabsorption of
uric acid
- renal calculi
- renal tubular acidosis type II
- reduced reabsorption of bicarbonate
- metabolic acidosis
- alkaline urine
- growth failure
- hypercalcuria
- reduced reabsorption of Ca2+
- nephrocalcinosis or renal stones
- distal tubule & collecting duct
- nephrogenic diabetes insipidus
- decreased H2O reabsorption
- polydipsia & polyuria
- fever
- failure to
thrive/poor
growth
- distal tubule
- Bartter syn
- reduced Cl- reabsorption
- hypokalaemic metabolic alkalosis
- hypercalciuria
- normal bp w/ raised renin
- polydipsia & polyuria
- growth
failure
- collecting duct
- renal tubular acidosis type I
- reduced secretion of H+
- metabolic acidosis
- alkaline urine
- growth failure
- nephrocalcinosis