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transient erythroblastopenia of childhood - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

transient erythroblastopenia of childhood

MONDO:0009197

Also known as:transient acquired pure red cell aplasiaerythroblastopenia, transientfamilial transient erythroblastopenia of childhood

Overview

An acquired pure red cell aplasia that is self-limited. It is the most common cause of decreased red blood cell production in the pediatric population, and typically presents as a normocytic anemia with reticulocytopenia in an otherwise asymptomatic and normal child with no evidence of other causes for anemia, including blood loss, hemolysis, nutritional deficiency, or malignancy.

GeneticsAutosomal recessive

ResearchLimited published research (4 articles)

Clinical Presentation

Features include: Transient erythroblastopenia and Low red blood cell count (anemia).

Organ System	Phenotype Count	Example Features
Blood and immune system	1	Low red blood cell count (anemia)

Explore clinical features

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for transient erythroblastopenia of childhood.

4 publications have been identified in PubMed for transient erythroblastopenia of childhood. Research spans Case Report / Case Series (75%) and Epidemiology / Natural History (25%).

Recent Publications

Patel S (2026). [PMID: 41658739](https://pubmed.ncbi.nlm.nih.gov/41658739/). *Cureus*. [Case Report / Case Series]
Rivetti G (2024). [PMID: 39075575](https://pubmed.ncbi.nlm.nih.gov/39075575/). *Italian journal of pediatrics*. [Case Report / Case Series]
Gunnes MW (2024). [PMID: 38506013](https://pubmed.ncbi.nlm.nih.gov/38506013/). *Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke*. [Case Report / Case Series]
Equitz E (2024). [PMID: 38554748](https://pubmed.ncbi.nlm.nih.gov/38554748/). *The Journal of pediatrics*. [Epidemiology / Natural History]

Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 8:31 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:227050

Orphanet

European rare disease database

Orphanet:98871

GARD

Genetic and Rare Diseases Info Center

GARD:7793

Questions for Your Care Team

→Should my partner and I meet with a genetic counselor to discuss carrier status and family planning?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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transient erythroblastopenia of childhood

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team