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.

Thoracic Hypoplasia at Birth as Presenting Feature of Shwachman-Diamond Syndrome in Twins / Capasso, Letizia; Borrelli, ANGELA CARLA; Cerullo, Julia; Pirozzi, Maria Rosaria; Raimondi, Francesco. - In: JOURNAL OF PEDIATRIC GENETICS. - ISSN 2146-4596. - 5:3(2016), pp. 158-60-160. [10.1055/s-0036-1584307]

Thoracic Hypoplasia at Birth as Presenting Feature of Shwachman-Diamond Syndrome in Twins

CAPASSO, LETIZIA;BORRELLI, ANGELA CARLA;CERULLO, JULIA;RAIMONDI, FRANCESCO
2016

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.
2016
Thoracic Hypoplasia at Birth as Presenting Feature of Shwachman-Diamond Syndrome in Twins / Capasso, Letizia; Borrelli, ANGELA CARLA; Cerullo, Julia; Pirozzi, Maria Rosaria; Raimondi, Francesco. - In: JOURNAL OF PEDIATRIC GENETICS. - ISSN 2146-4596. - 5:3(2016), pp. 158-60-160. [10.1055/s-0036-1584307]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/644960
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