Literature DB >> 8291513

Radiological features in Brachmann-de Lange syndrome.

S R Braddock1, R S Lachman, C C Stoppenhagen, J C Carey, M Ireland, J B Moeschler, C Cunniff, J M Graham.   

Abstract

Brachmann-de Lange syndrome (BDLS) is a well-delineated disorder consisting variably of pre- and postnatal growth deficiency, microbrachycephaly, characteristic face, hypertrichosis, visceral anomalies, and limb defects consisting primarily of variable limb reduction defects, micromelia, and elbow abnormalities. The course is usually marked by initial hypertonicity, low-pitched weak cry, feeding problems, and behavioral problems with marked mental deficiency. In classical cases there is rarely any difficulty in making the diagnosis, but for mildly affected cases, it may be difficult to feel secure about the diagnosis. In an effort to increase the precision of diagnosis for mildly affected cases, we reviewed roentgenograms in 21 cases of Brachmann-de Lange syndrome, as well as previously published descriptions of the radiological manifestations. Unusual radiologic manifestations were related primarily to the limb anomalies, and these were often asymmetric. These manifestations included digital abnormalities, which ranged from acheiria to oligodactyly, hypoplasia of the thumb and first metacarpal, clinodactyly of the fifth finger, or ectrodactyly. Long bone abnormalities included ulnar a/hypoplasia, dysplasia of the radial head, or fusion of the elbow. When there was a single forearm bone, there was often fusion at the elbow and oligodactyly, which made it difficult to determine whether the radius or ulna was absent. Other radiologic manifestations included 13 ribs with precocious sternal fusion, and micrognathia. We suggest that these radiologic manifestations could increase diagnostic precision in mildly affected cases.

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Year:  1993        PMID: 8291513     DOI: 10.1002/ajmg.1320470714

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  11 in total

Review 1.  Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): a review of 53 CdLS pregnancies.

Authors:  Dinah M Clark; Ilana Sherer; Matthew A Deardorff; Janice L B Byrne; Kathleen M Loomes; Malgorzata J M Nowaczyk; Laird G Jackson; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2012-06-27       Impact factor: 2.802

2.  Cornelia de Lange syndrome with additional clinical features and multicystic kidney disease.

Authors:  Jaiprakash Narayan Meghwal; Achala Arya; B S Karnawat; Suchitra Narayan
Journal:  Indian J Pediatr       Date:  2013-02-01       Impact factor: 1.967

3.  Neuroimaging features of Cornelia de Lange syndrome.

Authors:  Matthew T Whitehead; Usha D Nagaraj; Phillip L Pearl
Journal:  Pediatr Radiol       Date:  2015-02-21

4.  Cornelia de Lange Syndrome with NIPBL gene mutation: a case report.

Authors:  Kyung-Hee Park; Seung-Tae Lee; Chang-Seok Ki; Shin-Yun Byun
Journal:  J Korean Med Sci       Date:  2010-11-24       Impact factor: 2.153

5.  Genetic enhancement of limb defects in a mouse model of Cornelia de Lange syndrome.

Authors:  Martha E Lopez-Burks; Rosaysela Santos; Shimako Kawauchi; Anne L Calof; Arthur D Lander
Journal:  Am J Med Genet C Semin Med Genet       Date:  2016-04-27       Impact factor: 3.908

6.  Temporal bone CT findings in Cornelia de Lange syndrome.

Authors:  J Kim; E Y Kim; J S Lee; W S Lee; H N Kim
Journal:  AJNR Am J Neuroradiol       Date:  2007-12-07       Impact factor: 3.825

7.  Tracheomegaly in Brachmann-de Lange syndrome.

Authors:  M Grünebaum; L Kornreich; G Horev; N Ziv
Journal:  Pediatr Radiol       Date:  1996

8.  Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome.

Authors:  Shimako Kawauchi; Anne L Calof; Rosaysela Santos; Martha E Lopez-Burks; Clint M Young; Michelle P Hoang; Abigail Chua; Taotao Lao; Mark S Lechner; Jeremy A Daniel; Andre Nussenzweig; Leonard Kitzes; Kyoko Yokomori; Benedikt Hallgrimsson; Arthur D Lander
Journal:  PLoS Genet       Date:  2009-09-18       Impact factor: 5.917

9.  Dental findings in Cornelia de Lange syndrome.

Authors:  Aslihan Soyal Toker; Sinan Ay; Hasan Yeler; Ilhan Sezgin
Journal:  Yonsei Med J       Date:  2009-04-30       Impact factor: 2.759

Review 10.  Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.

Authors:  Antonie D Kline; Joanna F Moss; Angelo Selicorni; Anne-Marie Bisgaard; Matthew A Deardorff; Peter M Gillett; Stacey L Ishman; Lynne M Kerr; Alex V Levin; Paul A Mulder; Feliciano J Ramos; Jolanta Wierzba; Paola Francesca Ajmone; David Axtell; Natalie Blagowidow; Anna Cereda; Antonella Costantino; Valerie Cormier-Daire; David FitzPatrick; Marco Grados; Laura Groves; Whitney Guthrie; Sylvia Huisman; Frank J Kaiser; Gerritjan Koekkoek; Mary Levis; Milena Mariani; Joseph P McCleery; Leonie A Menke; Amy Metrena; Julia O'Connor; Chris Oliver; Juan Pie; Sigrid Piening; Carol J Potter; Ana L Quaglio; Egbert Redeker; David Richman; Claudia Rigamonti; Angell Shi; Zeynep Tümer; Ingrid D C Van Balkom; Raoul C Hennekam
Journal:  Nat Rev Genet       Date:  2018-10       Impact factor: 53.242

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