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

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder.

Pediatric nephrology (Berlin, Germany) - 1 Dec 2007

Sharma Ajay P, Greenberg Cheryl R, Prasad Asuri N, Prasad Chitra

Abstract excerpt

Diarrhea-positive hemolytic uremic syndrome (HUS) is a common cause of acute renal failure in children. Diarrhea-negative (D-), or atypical HUS, is etiologically distinct. A Medline search identified seven previously reported D- cases of HUS secondary to cobalamin C (cblC) disease presenting in infancy. An infantile presentation is reported to be associated with a high mortality rate (6/7 cases). We describe the...

Read the complete abstract on PubMed

Topics

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

Share to Acute Kidney Injury
Share to Betaine
Share to Brain Diseases, Metabolic, Inborn

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

Share to Carnitine

Share to Hemolytic-Uremic Syndrome

Share to Homocystinuria

Share to Methylmalonic Acid

Share to Proto-Oncogene Proteins c-cbl

Source

Identifiers

PMID: 17874135
DOI: 10.1007/s00467-007-0604-1

Genes

MMACHC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder.PMID 17874135Read ↗

Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children.Semantic proximity Read ↗

Late-onset Renal involvement presenting with TMA and tubular injury in cobalamin C disease: a report of three cases and review of the literatureSemantic proximity Read ↗

Cobalamin C defect-hemolytic uremic syndrome caused by new mutation in MMACHC.Semantic proximity Read ↗

CblC Deficiency is the Cause of Persistent Proteinuria in a Young Female Ten Years After the Diagnosis of Atypical Nephropathy: A Case ReportSemantic proximity Read ↗

Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutation.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review.Semantic proximity Read ↗

Clinical feature and outcome of late-onset cobalamin C disease patients with neuropsychiatric presentations: a Chinese case seriesSemantic proximity Read ↗

Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.Semantic proximity Read ↗

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.Semantic proximity Read ↗

Cobalamin C deficiency presenting with diffuse alveolar hemorrhage and pulmonary microangiopathy.Semantic proximity Read ↗

A case of carbamoyl phosphate synthetase 1 deficiency presenting symptoms at one month of age.Semantic proximity Read ↗

Congenital intestinal atresias with multiple episodes of sepsis: A case report and review of literature.Semantic proximity Read ↗

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