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Abnormal circulating ceruloplasmin concentration

MedGen UID:
1726009
Concept ID:
C5421638
Finding
HPO: HP:0033144

Definition

Any deviation of the concentration of ceruloplasmin in the blood from the normal range. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAbnormal circulating ceruloplasmin concentration

Conditions with this feature

Hemochromatosis type 5
MedGen UID:
341982
Concept ID:
C1851316
Disease or Syndrome
A rare disorder of iron metabolism and transport characterised by elevated serum ferritin levels, increased serum iron, increased transferrin saturation and heavy iron deposition in hepatocytes. Iron deposition has also been indicated in heart and bone marrow, while haematological examination of peripheral blood shows no abnormalities.
Neurodegeneration and seizures due to copper transport defect
MedGen UID:
1841021
Concept ID:
C5830385
Disease or Syndrome
Neurodegeneration and seizures due to copper transport defect (NSCT) is an autosomal recessive disorder of copper transport characterized by hypotonia, global developmental delay, seizures, and rapid brain atrophy (summary by Dame et al., 2023).

Recent clinical studies

Etiology

Kirschbaum B
Biol Trace Elem Res 2000 Oct;77(1):13-24. doi: 10.1385/BTER:77:1:13. PMID: 11097467
Roels H, Lauwerys R, Buchet JP, Genet P, Sarhan MJ, Hanotiau I, de Fays M, Bernard A, Stanescu D
Am J Ind Med 1987;11(3):307-27. doi: 10.1002/ajim.4700110308. PMID: 3578289

Diagnosis

Guindi M
Semin Diagn Pathol 2019 Nov;36(6):415-422. Epub 2019 Jul 25 doi: 10.1053/j.semdp.2019.07.008. PMID: 31421978
Roels H, Lauwerys R, Buchet JP, Genet P, Sarhan MJ, Hanotiau I, de Fays M, Bernard A, Stanescu D
Am J Ind Med 1987;11(3):307-27. doi: 10.1002/ajim.4700110308. PMID: 3578289

Therapy

Roels H, Lauwerys R, Buchet JP, Genet P, Sarhan MJ, Hanotiau I, de Fays M, Bernard A, Stanescu D
Am J Ind Med 1987;11(3):307-27. doi: 10.1002/ajim.4700110308. PMID: 3578289

Clinical prediction guides

Kirschbaum B
Biol Trace Elem Res 2000 Oct;77(1):13-24. doi: 10.1385/BTER:77:1:13. PMID: 11097467

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