Transient erythroblastopenia of childhood in siblings: Case report and review of the literature

Journal of Pediatric Hematology/Oncology

Volumn 29, Issue 9, 2007, Pages 659-660

  Shaw, Jordan ^a   Meeder, Robert ^a  

^a Orillia Soldiers' Memorial Hospital   (Canada)

Author keywords

Anemia; TEC; Transient erythroblastopenia of childhood

Indexed keywords

IRON;

ARTICLE; BLOOD SMEAR; BONE MARROW BIOPSY; CASE REPORT; CHILD; CLINICAL FEATURE; DISEASE COURSE; ERYTHROBLASTOPENIA; ERYTHROCYTE TRANSFUSION; HUMAN; IRON DEFICIENCY; MALE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SIBLING; TRANSIENT ERYTHROBLASTOPENIA;

ANEMIA, APLASTIC; ERYTHROBLASTS; ERYTHROPOIESIS; HUMANS; INFANT; MALE; SIBLINGS;

EID: 34548433427     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e31814684e9     Document Type: Article

References (6)

1. Labotka RJ, Maurer HS, Honig GR. Transient erythroblastopenia of childhood: review of 17 cases, including a pair of identical twins. Am J Dis Child. 1981;135:937-940.
2. Seip M. Transient erythroblastopenia in siblings. Acta Pediatr Scand. 1982;71:689-690.
3. Glader BE. Diagnosis and management of red cell aplasia in children. Hemat/Oncol Clin N Am. 1987;1:431-447.
4. Skeppner G, Forestier E, Henter J-I, et al. Transient red cell aplasia in siblings: a common environmental or a common hereditary factor? Acta Paediatr. 1998;87:43-47.
5. Gustavsson P, Klar J, Matsson H, et al. Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene. Br J Haem. 2002;119:261-264.
6. Rao SP, Miller ST, Brown AK. Transient erythroblastopenia of childhood in two pairs of siblings. Ped Res. 1990;27:148a.