| Literature DB >> 27617157 |
Letizia Capasso1, Angela Carla Borrelli1, Julia Cerullo1, Maria Rosaria Pirozzi1, Francesco Raimondi1.
Abstract
Shwachman-Diamond syndrome (SDS) is a rare autosomal recessive disorder of marrow failure syndrome and exocrine pancreatic dysfunction with an estimated incidence of 1/76,000. When present, characteristic skeletal abnormalities are strongly suggestive of SDS but most often they are seen during childhood and adolescence. We present a case of preterm twins with prenatal diagnosis of thoracic hypoplasia and a clinical evolution that lead to an early diagnosis of SDS. This report highlights the importance of a high index of suspicion for SDS in case of neonatal thoracic hypoplasia.Entities:
Keywords: exocrine pancreatic dysfunction; limb shortness; neutropenia; newborn; thoracic hypoplasia
Year: 2016 PMID: 27617157 PMCID: PMC4999326 DOI: 10.1055/s-0036-1584307
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X