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

Clinical Presentation of a Patient With Hemochromatosis After Bariatric Surgery With HFE (H63D) Mutation.

Journal of investigative medicine high impact case reports - 1 Jan 2026

Petridis Samuele, Rodriguez Karla Baez, Punjabi Naresh, De La Cruz-Munoz Nestor, Bernal-Mizrachi Ernesto, Varghese Ron T

Abstract excerpt

Hereditary hemochromatosis (HH) is a genetic disorder characterized by excessive intestinal iron absorption, most associated with HFE C282Y homozygosity. In contrast, H63D homozygosity is considered a low-penetrance genotype that rarely leads to clinically significant iron overload. Bariatric surgery, particularly sleeve gastrectomy, may predispose patients to iron deficiency through reduced gastric acid and...

Read the complete abstract on PubMed

Topics

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

Share to Homozygote
Share to Bariatric Surgery

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to F3 gene

Share to HFE gene

Share to Hemochromatosis

Share to Hemochromatosis Protein

Share to Mutation

Share to Obesity, Morbid

Source

Open in PubMed Open full text

Identifiers

PMID: 42572894
DOI: 10.1177/23247096261433343
PMCID: PMC13009573

Genes

HFE
F3

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Presentation of a Patient With Hemochromatosis After Bariatric Surgery With HFE (H63D) Mutation.PMID 42572894Read ↗

Clinical characteristics of HFE C282Y/H63D compound heterozygotes identified in a specialty practice: key differences from HFE C282Y homozygotes.Semantic proximity Read ↗

H63D Syndrome: A rare clinical phenotype caused by a homozygous mutation of HFE gene H63DSemantic proximity Read ↗

Haemochromatosis: a clinical update for the practising physician.Semantic proximity Read ↗

Endocrine dysfunction in hereditary hemochromatosis.Semantic proximity Read ↗

Hemochromatosis: an endocrine liver disease.Semantic proximity Read ↗

[Diagnosis of haemochromatosis].Semantic proximity Read ↗

Hemochromatosis, alcoholism and unhealthy dietary fat: a case report.Semantic proximity Read ↗

Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review.Semantic proximity Read ↗

Hemochromatosis is successfully controlled with Bariatric Surgery – Report of two Cases with long-term follow-upSemantic proximity Read ↗

Phenotypic and clinical manifestations of compound heterozygous genetic haemochromatosis (CHGH): a non-invasive approach to clinical management.Semantic proximity Read ↗

The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.Semantic proximity Read ↗

Hereditary hemochromatosis: missed diagnosis or misdiagnosis?Semantic proximity Read ↗

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