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

[Hereditary hyperferritinemia-cataract syndrome. Unusual differential diagnosis of unexplainable high levels of ferritin].

Lakartidningen - 1 Jan 2000

Vaktnäs Johan, Olsson Mikael

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Apoferritins
Share to Cataract
Share to Diagnosis, Differential
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Iron Metabolism Disorders

Share to Mutation

Source

Identifiers

PMID: 24501909

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Hereditary hyperferritinemia-cataract syndrome. Unusual differential diagnosis of unexplainable high levels of ferritin].PMID 24501909Read ↗

Hyperferritinaemia-cataract syndrome.Semantic proximity Read ↗

[Hereditary hyperferritinemia cataract syndrome].Semantic proximity Read ↗

[Hereditary hyperferritinemia cataract syndrome--the first family in Germany].Semantic proximity Read ↗

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

[Molecular genetics of hereditary cataract-hyperferritinemia syndrome].Semantic proximity Read ↗

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

Ferritin L-subunit Gene Mutation and Hereditary Hyperferritinaemia Cataract Syndrome: A Case Report and Literature Review Semantic proximity Read ↗

Pathogenesis of Hyperferritinemia Cataract SyndromeSemantic proximity Read ↗

Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.Semantic proximity Read ↗

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

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

Novel ferritin L-chain gene variant in a case of hereditary hyperferritinemia-cataract syndrome without family history.Semantic proximity Read ↗

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