Loeys-Dietz syndrome presenting as respiratory distress due to pulmonary artery dilation.

Autor: Kuppler KM; Wake Forest School of Medicine, Winston-Salem, North Carolina 27157, USA., Kirse DJ, Thompson JT, Haldeman-Englert CR
Jazyk: angličtina
Zdroj: American journal of medical genetics. Part A [Am J Med Genet A] 2012 May; Vol. 158A (5), pp. 1212-5. Date of Electronic Publication: 2012 Apr 09.
DOI: 10.1002/ajmg.a.35274
Abstrakt: Loeys-Dietz syndrome (LDS) is an autosomal dominant connective tissue condition with clinical features that may include ocular hypertelorism, cleft palate, craniosynostosis, and vascular dilation and tortuosity. Here we describe a patient with LDS confirmed by genetic analysis (R528H mutation of TGFBR2) who presented at 3 months of age in respiratory distress of unknown origin. In addition to expressing several of the classic findings of LDS, including a novel finding of squamosal suture craniosynostosis, CT angiography revealed aortic dilation at the sinus of valsalva, pulmonary artery dilation that extrinsically compressed the right mainstem bronchus causing bronchomalacia, and an apical herniation of the right lung. This is the first documentation of concomitant airway and pulmonary findings in a patient with LDS. We suggest that (1) vascular abnormalities be considered as a cause of unexplained respiratory distress in a patient with LDS, and (2) pediatric patients exhibiting any of the physical findings listed above be evaluated for LDS with particular attention paid to vascular, airway, and/or pulmonary malformations.
(Copyright © 2012 Wiley Periodicals, Inc.)
Databáze: MEDLINE
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