Literature DB >> 12878302

Neurocristopathies presenting with neurologic abnormalities associated with Hirschsprung's disease.

Eli Shahar1, Maruan Shinawi.   

Abstract

Neurocristopathies are a group of diverse disorders resulting from defective growth, differentiation, and migration of the neural crest cells. Hirschsprung's disease, namely aganglionic megacolon, is the consequence of defective migration of neural crest cells on to the colonic submucosa and is therefore considered a neurocristopathy. We report on four children in whom was diagnosed a neurocristopathy, associating Hirschsprung's disease with a wide spectrum of neurologic abnormalities. The patients included two children presenting the phenotypic features of the Goldberg-Shprintzen syndrome: distinct dysmorphic facial features, microcephaly, and mental retardation, along with agenesis of the corpus callosum and cortical malformations associated with intractable seizures in one child. The third newborn presented with the Haddad syndrome: short-segment Hirschsprung's disease associated with the congenital central hypoventilation syndrome requiring permanent artificial ventilation. In the fourth child, absence of the corpus callosum was associated with mild dysmorphic features, borderline cognitive abilities, and attention-deficit disorder. Therefore, awareness of a possible neurocristopathy associated with neurologic abnormalities should be taken into account in any patient newly diagnosed with Hirschsprung's disease to detect the abnormalities early and promptly manage them. A thorough neurologic examination and a developmental assessment, including magnetic resonance imaging of the brain and electroencephalography, should be performed for any child presenting with an aganglionic megacolon, especially those presenting with seizures, developmental delay, or even congenital hypoventilation.

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Year:  2003        PMID: 12878302     DOI: 10.1016/s0887-8994(03)00010-9

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  7 in total

Review 1.  Prevalence of Hirschsprung's disease in premature infants: a systematic review.

Authors:  Johannes W Duess; Alejandro D Hofmann; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-07-02       Impact factor: 1.827

Review 2.  Hirschsprung's disease and the brain.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2010-12-05       Impact factor: 1.827

3.  miR-100 rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children.

Authors:  Yun Zhu; Ao Lin; Yi Zheng; Xiaoli Xie; Qiuming He; Wei Zhong
Journal:  Pharmgenomics Pers Med       Date:  2020-08-10

Review 4.  Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2012-09-23       Impact factor: 1.827

Review 5.  The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2006-03-04       Impact factor: 1.827

Review 6.  Hirschsprung's disease: clinical dysmorphology, genes, micro-RNAs, and future perspectives.

Authors:  Consolato Maria Sergi; Oana Caluseriu; Hunter McColl; David D Eisenstat
Journal:  Pediatr Res       Date:  2016-09-28       Impact factor: 3.756

7.  Rare association of Hirschsprung's disease and Joubert syndrome.

Authors:  Hamit Ozyurek; Ozlem Eroglu Kayacik; Olcay Gungor; Filiz Karagoz
Journal:  Eur J Pediatr       Date:  2007-05-22       Impact factor: 3.183

  7 in total

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