Indication
Lead toxicity
Lead toxicity is a multi-system pathological state caused by the absorption and systemic accumulation of the toxic heavy metal lead. Read more about Lead toxicity
6 drugs 6 manufacturers
Drugs that treat it
Common Lead toxicity therapies.
BAL IN OIL (dimercaprol)
CHEMET (succimer)
EDETATE CALCIUM DISODIUM
EDETATE CALCIUM DISODIUM
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonLead toxicity is a multi-system pathological state caused by the absorption and systemic accumulation of the toxic heavy metal lead.
It affects both children and adults, though pediatric populations are particularly vulnerable to neurodevelopmental damage.
Pathophysiologically, lead mimics divalent cations such as calcium, binds to sulfhydryl-containing proteins, and disrupts enzymatic processes—notably inhibiting delta-aminolevulinic acid dehydratase and ferrochelatase in the heme synthesis pathway.
Clinical manifestations vary with exposure duration and blood lead concentration, ranging from insidious neurocognitive deficits, fatigue, and microcytic anemia to acute lead colic, peripheral motor neuropathy, chronic nephropathy, encephalopathy, and seizures.
- nih.gov
Lead toxicity is a multi-system pathological state caused by the absorption and systemic accumulation of the toxic heavy metal lead
- nih.gov
Lead toxicity is a multi-system pathological state caused by the absorption and systemic accumulation of the toxic heavy metal lead
- nih.gov
It affects both children and adults, though pediatric populations are particularly vulnerable to neurodevelopmental damage Pathophysiologically, lead mimics divalent cations such as calcium, binds to sulfhydryl-containing proteins, and disrupts enzymatic processes—notably inhibiting delta-aminolevulinic acid dehydratase and ferrochelatase in the heme synthesis pathway Clinical manifestations vary with exposure duration and blood lead concentration, ranging from insidious neurocognitive deficits,...
- nih.gov
It affects both children and adults, though pediatric populations are particularly vulnerable to neurodevelopmental damage
- nih.gov
Pathophysiologically, lead mimics divalent cations such as calcium, binds to sulfhydryl-containing proteins, and disrupts enzymatic processes—notably inhibiting delta-aminolevulinic acid dehydratase and ferrochelatase in the heme synthesis pathway
- nih.gov
Clinical manifestations vary with exposure duration and blood lead concentration, ranging from insidious neurocognitive deficits, fatigue, and microcytic anemia to acute lead colic, peripheral motor neuropathy, chronic nephropathy, encephalopathy, and seizures
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