Literature DB >> 8291519

Gastrointestinal abnormalities: a significant cause of feeding difficulties and failure to thrive in Brachmann-de Lange syndrome.

M J Bull1, J F Fitzgerald, S A Heifetz, T J Brei.   

Abstract

Gastroesophageal abnormalities occur with increased frequency in patients with Brachmann-de Lange syndrome (BDLS) and contribute to problems with feeding, emesis and failure to thrive. Comprehensive evaluation including longitudinal assessment of growth and development of 8 patients with BDLS was performed. Clinically significant feeding problems occurred in 6 of the 8 patients and the affected children were subsequently evaluated for gastrointestinal abnormalities. Findings in these patients included tracheal aspiration, esophageal dysmotility, gastroesophageal reflux, hiatal hernia, and esophagitis. Medical treatment was instituted where appropriate, and surgical treatment was performed if the problems did not resolve with medical treatment. Improvement in weight centiles occurred in all patients fed by nasogastric or feeding gastrostomy tube but only one patient appeared to experience increase in rate of linear growth. Careful monitoring of symptoms and growth parameters, and prompt institution of appropriate medical and surgical measures can improve the health and physical outcome of many patients with BDLS.

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Year:  1993        PMID: 8291519     DOI: 10.1002/ajmg.1320470720

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


  6 in total

1.  Classical cornelia de lange syndrome.

Authors:  Ev Badoe
Journal:  Ghana Med J       Date:  2006

2.  Case 3: Emesis in a Term Infant with Dysmorphic Features.

Authors:  Tadarro Lee Richardson; Meaghan Ransom; Gabriella Crane; Erin Plosa; Jennifer Sucre
Journal:  Neoreviews       Date:  2020-02

3.  Aesthetic and functional management of a patient with Cornelia de Lange syndrome.

Authors:  Dexton Antony Johns; Dnyanesh L Bhonsale; V Y Shivashanker; Manu Johns
Journal:  Contemp Clin Dent       Date:  2012-04

4.  Anesthetic management of a child with Cornelia de Lange Syndrome undergoing open heart surgery: A case report.

Authors:  Oguzhan Arun; Bahar Oc; Esma Nur Metin; Ahmet Sert; Resul Yilmaz; Mehmet Oc
Journal:  World J Cardiol       Date:  2022-01-26

5.  Cornelia de Lange Syndrome: A Newborn with Imperforate Anus and a NIPBL Mutation.

Authors:  Rose H Mende; David P Drake; Raimos M Olomi; Ben C J Hamel
Journal:  Case Rep Genet       Date:  2012-12-10

Review 6.  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

  6 in total

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