Literature DB >> 27853988

Antenatal manifestations of inborn errors of metabolism: prenatal imaging findings.

Laurent Guibaud1,2,3, Sophie Collardeau-Frachon4, Audrey Lacalm5, Mona Massoud6, Massimiliano Rossi7, Marie Pierre Cordier7, Christine Vianey-Saban8.   

Abstract

Prenatal manifestations of inborn errors of metabolism (IEM) are related to severe disorders involving metabolic pathways active in the fetal period and not compensated by maternal or placental metabolism. Some prenatal imaging findings can be suggestive of such conditions-especially in cases of consanguinity and/or recurrence of symptoms-after exclusion of the most frequent nonmetabolic etiologies. Most of these prenatal imaging findings are nonspecific. They include mainly ascites and hydrops fetalis, intrauterine growth restriction (IUGR), central nervous system (CNS) anomalies, echogenic kidneys, epiphyseal stippling, craniosynostosis, and a wide spectrum of dysostoses. These anomalies can be isolated, but in most cases, an IEM is suggested by an association of features. It must be stressed that the diagnosis of an IEM in the prenatal period is based on a close collaboration between specialists in fetal imaging, medicine, genetics, biology, and pathology.

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Year:  2016        PMID: 27853988     DOI: 10.1007/s10545-016-9992-3

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  56 in total

Review 1.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2011-10-07       Impact factor: 4.797

2.  Isolated hyperechoic fetal colon before 36 weeks' gestation reveals cystinuria.

Authors:  S Amat; I Czerkiewicz; J-F Benoist; D Eurin; M Fontanges; F Muller
Journal:  Ultrasound Obstet Gynecol       Date:  2011-11       Impact factor: 7.299

Review 3.  Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis.

Authors:  Massimiliano Rossi; Christine M Hall; Raymonde Bouvier; Sophie Collardeau-Frachon; Frédérique Le Breton; Martine Bucourt; Marie Pierre Cordier; Christine Vianey-Saban; Giancarlo Parenti; Generoso Andria; Martine Le Merrer; Patrick Edery; Amaka C Offiah
Journal:  Pediatr Radiol       Date:  2015-02-03

4.  Diagnostic pitfall in antenatal manifestations of CPT II deficiency.

Authors:  F Boemer; M Deberg; R Schoos; J-H Caberg; S Gaillez; C Dugauquier; K Delbecque; A François; P Maton; N Demonceau; G Senterre; S Ferdinandusse; F-G Debray
Journal:  Clin Genet       Date:  2015-05-05       Impact factor: 4.438

5.  Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero.

Authors:  R Froissart; D Cheillan; R Bouvier; S Tourret; V Bonnet; M Piraud; I Maire
Journal:  J Med Genet       Date:  2005-04-01       Impact factor: 6.318

6.  Hyper-echogenic colon: a prenatal sign of cystinuria?

Authors:  M Brasseur-Daudruy; C Garel; V Brossard; F Broux; B Heckettsweiler; D Eurin
Journal:  Prenat Diagn       Date:  2006-12       Impact factor: 3.050

Review 7.  Prenatal Imaging of Craniosynostosis Syndromes.

Authors:  Pamela Deaver Ketwaroo; Caroline D Robson; Judy A Estroff
Journal:  Semin Ultrasound CT MR       Date:  2015-06-16       Impact factor: 1.875

Review 8.  Antenatal manifestations of Smith-Lemli-Opitz (RSH) syndrome: a retrospective survey of 30 cases.

Authors:  Alice Goldenberg; Claude Wolf; Françoise Chevy; Alexandra Benachi; Yves Dumez; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Med Genet A       Date:  2004-02-01       Impact factor: 2.802

9.  Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.

Authors:  C G Steward; R A Newbury-Ecob; R Hastings; S F Smithson; B Tsai-Goodman; O W Quarrell; W Kulik; R Wanders; M Pennock; M Williams; J L Cresswell; I L Gonzalez; P Brennan
Journal:  Prenat Diagn       Date:  2010-10       Impact factor: 3.050

10.  Prenatal Diagnosis of Antley-Bixler Syndrome and POR Deficiency.

Authors:  Elena Oldani; Catherine Garel; Martine Bucourt; Lionel Carbillon
Journal:  Am J Case Rep       Date:  2015-12-16
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  1 in total

Review 1.  Contribution of tandem mass spectrometry to the diagnosis of lysosomal storage disorders.

Authors:  Monique Piraud; Magali Pettazzoni; Pamela Lavoie; Séverine Ruet; Cécile Pagan; David Cheillan; Philippe Latour; Christine Vianey-Saban; Christiane Auray-Blais; Roseline Froissart
Journal:  J Inherit Metab Dis       Date:  2018-03-19       Impact factor: 4.982

  1 in total

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