Pediatrics International | 2021

Segmental multicystic dysplastic kidney: Two case reports

 
 
 
 
 

Abstract


1 Duran M, Hofkamp M, Rhead WJ, Saudubray JM, Wadman SK. Sudden child death and “healthy” affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency. Pediatrics 1986; 78: 1052–7. 2 Li Y, Zhu R, Liu Y, Song J, Xu J, Yang Y. Medium-chain acyl-coenzyme A dehydrogenase deficiency: six cases in the Chinese population. Pediatr. Int. 2019; 61: 551–7. 3 Wilcken B, Haas M, Joy P et al. Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study. Lancet 2007; 369: 37– 42. 4 Purevsuren J, Hasegawa Y, Fukuda S et al. Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency. Mol. Genet. Metab. 2012; 107: 237–40. 5 Tajima G, Hara K, Tsumura M et al. Screening of MCAD deficiency in Japan: 16 years’ experience of enzymatic and genetic evaluation. Mol. Genet. Metab. 2016; 119: 322–8.

Volume 63
Pages None
DOI 10.1111/ped.14593
Language English
Journal Pediatrics International

Full Text