Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Hyperferritinaemia not always a sign of iron overload.

Acta gastro-enterologica Belgica - 1 Jan 2000

Loffeld R J L F

Abstract excerpt

The level of serum ferritin normally parallels the concentration of storage iron within the body. In the absence of chronic diseases elevated serum ferritin levels will lead to the diagnosis congenital haemochromatosis. However, there are genetic disorders with high ferritin levels without any sign of iron overload. A case history of a patient suffering from cataract at young age and high ferritin levels is...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Ferritins
Share to Guanine
Share to Cataract

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytosine

Share to Iron Metabolism Disorders

Share to Mutation

Share to Syndrome

Source

Identifiers

PMID: 18330093

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hyperferritinaemia not always a sign of iron overload.PMID 18330093Read ↗

Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.Semantic proximity Read ↗

Hyperferritinaemia-cataract syndrome.Semantic proximity Read ↗

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome.Semantic proximity Read ↗

The hereditary hyperferritinemia-cataract syndrome: a family study.Semantic proximity Read ↗

Hereditary hyperferritinaemia-cataract syndrome: a challenging diagnosis for the hepatogastroenterologist.Semantic proximity Read ↗

Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations.Semantic proximity Read ↗

Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 families.Semantic proximity Read ↗

Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family.Semantic proximity Read ↗

Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia.Semantic proximity Read ↗

Hereditary hyperferritinemia-cataract syndrome in three Czech families: molecular genetic testing and clinical implications.Semantic proximity Read ↗

Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.Semantic proximity Read ↗

Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.