Pearson Syndrome: A Rare Cause of Failure to Thrive in Infants

Clin Pediatr (Phila). 2019 Jun;58(7):819-824. doi: 10.1177/0009922819834285. Epub 2019 Mar 7.

Authors

Lauren Pronman^{1

2}, Monica Rondinelli^{1

2}, Deepika D'Cunha Burkardt¹, Sujithra Velayuthan^{1

2}, Ali Salar Khalili^{1

2}, Jirair K Bedoyan^{1

2

3}

Affiliations

¹ 1 University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
² 2 Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
³ 3 Case Western Reserve University, Cleveland, OH, USA.

PMID: 30845838
DOI: 10.1177/0009922819834285

No abstract available

Publication types

Case Reports

MeSH terms

Acyl-CoA Dehydrogenase, Long-Chain / deficiency*
Congenital Bone Marrow Failure Syndromes / complications*
Congenital Bone Marrow Failure Syndromes / diagnosis*
Diagnosis, Differential
Failure to Thrive / etiology*
Failure to Thrive / therapy
Humans
Infant
Lipid Metabolism, Inborn Errors / complications*
Lipid Metabolism, Inborn Errors / diagnosis*
Mitochondrial Diseases / complications*
Mitochondrial Diseases / diagnosis*
Muscular Diseases / complications*
Muscular Diseases / diagnosis*

Substances

Acyl-CoA Dehydrogenase, Long-Chain

Supplementary concepts

VLCAD deficiency