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.

Pulmonary hypoplasia

Total: 2

(per page)

PMID (PMCID)
15061322	MALE	Infant, Newborn
	Pulmonary hypoplasia and persistent pulmonary hypertension in the newborn with homozygous alpha-thalassemia: a case report and review of the literature.
	Bizzarro MJ, Copel JA, Pearson HA, Pober B, Bhandari V. J Matern Fetal Neonatal Med. 2003;14(6):411-6.
	Pulmonary hypoplasia and persistent pulmonary hypertension in the newborn with homozygous alpha-thalassemia: a case report and review of the literature.
15061322	MALE	Infant, Newborn
	Pulmonary hypoplasia and persistent pulmonary hypertension in the newborn with homozygous alpha-thalassemia: a case report and review of the literature.
	Bizzarro MJ, Copel JA, Pearson HA, Pober B, Bhandari V. J Matern Fetal Neonatal Med. 2003;14(6):411-6.
	We report the survival of a newborn with homozygous alpha-thalassemia complicated by pulmonary hypoplasia and persistent pulmonary hypertension, an association not previously reported.