Literature DB >> 12784293

Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptoms.

S Luzzani1, F Macchini, A Valadè, D Milani, A Selicorni.   

Abstract

As previously reported, gastroesophageal reflux (GER) is a frequent and severe medical complication of Cornelia de Lange syndrome (CDLS). The incidence of GER and the correlation between its presence and degree, and the clinical phenotype of CDLS (mild/classical according to Van Allen classification) were evaluated in a series of 43 patients. The pattern of presenting symptoms and their clinical evolution after medical or surgical treatment were also studied. A pathological GER was evident in 28/43 (65%) CDLS patients. The incidence of the complication was not significantly different in patients with classical (93.3%) vs. mild phenotype (82.3%), whereas a strong correlation was present between the degree of the esophageal damage and the clinical phenotype. A behavioral symptom (hyperactivity) was the most frequent sign associated with the condition (85%). Our data confirm the high occurrence of GER in CDLS patients, independently from the CDLS clinical phenotype. Regarding the severity of the esophageal lesions, a significant difference between the two clinical CDLS phenotypes was found. The evaluation of the presenting symptoms and of their evolution during the treatment emphasizes the importance of behavioral symptoms as major signs of esophageal damage in CDLS. Copyright 2003 Wiley-Liss, Inc.

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Mesh:

Year:  2003        PMID: 12784293     DOI: 10.1002/ajmg.a.20191

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  26 in total

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2.  Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance.

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3.  Predictors of Self-Injurious Behavior and Self-Restraint in Autism Spectrum Disorder: Towards a Hypothesis of Impaired Behavioral Control.

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Review 6.  Self-injurious behaviour in intellectual disability syndromes: evidence for aberrant pain signalling as a contributing factor.

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8.  Neuroimaging features of Cornelia de Lange syndrome.

Authors:  Matthew T Whitehead; Usha D Nagaraj; Phillip L Pearl
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Review 9.  Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome.

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

10.  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

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