Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Alpha-thalassemia

An inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles.

Megaloblastic bone marrow

Abnormal increased number of megaloblasts in the bone marrow.

Total: 1

(per page)

PMID (PMCID)
17412572	MIXED_SAMPLE	Infant
	[Failure to thrive and psychomotor regression revealing vitamin B12 deficiency in 3 infants].
	Mathey C, Di Marco JN, Poujol A, Cournelle MA, Brevaut V, Livet MO, Chabrol B, Michel G. Arch Pediatr. 2007;14(5):467-71.
	Blood cell count showed a macrocytosis without anemia (case 2-3) and a severe microcytic anemia for the first case caused by a mild alpha-thalassemia, with megaloblastic bone marrow.