Literature DB >> 17516083

Rare association of Hirschsprung's disease and Joubert syndrome.

Hamit Ozyurek1, Ozlem Eroglu Kayacik, Olcay Gungor, Filiz Karagoz.   

Abstract

We present the case of an 18-month-old boy with Hirschsprung's disease who had psychomotor retardation. His clinical and radiological findings were consistent with Joubert syndrome. The patient was the second case to show the association between Hirschsprung's disease and Joubert syndrome in the literature. As in our case, association of these entities by chance seems to be unlikely. Genetic analysis of new Joubert syndrome and Hirschsprung's disease patients may identify the candidate genes.

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Year:  2007        PMID: 17516083     DOI: 10.1007/s00431-007-0504-1

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  9 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome.

Authors:  M A Parisi; D Doherty; M L Eckert; D W W Shaw; H Ozyurek; S Aysun; O Giray; A Al Swaid; S Al Shahwan; N Dohayan; E Bakhsh; O S Indridason; W B Dobyns; C L Bennett; P F Chance; I A Glass
Journal:  J Med Genet       Date:  2005-09-09       Impact factor: 6.318

Review 3.  Genetic basis of Joubert syndrome and related disorders of cerebellar development.

Authors:  Carrie M Louie; Joseph G Gleeson
Journal:  Hum Mol Genet       Date:  2005-10-15       Impact factor: 6.150

4.  Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation.

Authors:  M Joubert; J J Eisenring; J P Robb; F Andermann
Journal:  Neurology       Date:  1969-09       Impact factor: 9.910

5.  Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance.

Authors:  B L Maria; R G Quisling; L C Rosainz; A T Yachnis; J Gitten; D Dede; E Fennell
Journal:  J Child Neurol       Date:  1999-06       Impact factor: 1.987

6.  Hirschsprung-associated congenital anomalies.

Authors:  A Sarioglu; F C Tanyel; N Büyükpamukçu; A Hiçsönmez
Journal:  Eur J Pediatr Surg       Date:  1997-12       Impact factor: 2.191

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

Authors:  Eli Shahar; Maruan Shinawi
Journal:  Pediatr Neurol       Date:  2003-05       Impact factor: 3.372

Review 8.  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

9.  Hemimegalencephaly and Hirschsprung's disease: a unique association.

Authors:  D Türkdoğan-Sözüer; M M Ozek; V Sehiralti; O Kurtkaya; A Sav
Journal:  Pediatr Neurol       Date:  1998-05       Impact factor: 3.372

  9 in total
  6 in total

Review 1.  Joubert Syndrome and related disorders.

Authors:  Francesco Brancati; Bruno Dallapiccola; Enza Maria Valente
Journal:  Orphanet J Rare Dis       Date:  2010-07-08       Impact factor: 4.123

Review 2.  Healthcare recommendations for Joubert syndrome.

Authors:  Ruxandra Bachmann-Gagescu; Jennifer C Dempsey; Sara Bulgheroni; Maida L Chen; Stefano D'Arrigo; Ian A Glass; Theo Heller; Elise Héon; Friedhelm Hildebrandt; Nirmal Joshi; Dana Knutzen; Hester Y Kroes; Stephen H Mack; Sara Nuovo; Melissa A Parisi; Joseph Snow; Angela C Summers; Jordan M Symons; Wadih M Zein; Eugen Boltshauser; John A Sayer; Meral Gunay-Aygun; Enza Maria Valente; Dan Doherty
Journal:  Am J Med Genet A       Date:  2019-11-11       Impact factor: 2.802

3.  Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease.

Authors:  Loïc de Pontual; Norann A Zaghloul; Sophie Thomas; Erica E Davis; David M McGaughey; Hélène Dollfus; Clarisse Baumann; Seneca L Bessling; Candice Babarit; Anna Pelet; Cecilia Gascue; Philip Beales; Arnold Munnich; Stanislas Lyonnet; Heather Etchevers; Tania Attie-Bitach; Jose L Badano; Andrew S McCallion; Nicholas Katsanis; Jeanne Amiel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-31       Impact factor: 11.205

4.  Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Authors:  Andrea Poretti; Giuseppina Vitiello; Raoul C M Hennekam; Filippo Arrigoni; Enrico Bertini; Renato Borgatti; Francesco Brancati; Stefano D'Arrigo; Francesca Faravelli; Lucio Giordano; Thierry A G M Huisman; Miriam Iannicelli; Gerhard Kluger; Marten Kyllerman; Magnus Landgren; Melissa M Lees; Lorenzo Pinelli; Romina Romaniello; Ianina Scheer; Christoph E Schwarz; Ronen Spiegel; Daniel Tibussek; Enza Maria Valente; Eugen Boltshauser
Journal:  Orphanet J Rare Dis       Date:  2012-01-11       Impact factor: 4.123

5.  Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling.

Authors:  Thuy-Linh Le; Yunia Sribudiani; Xiaomin Dong; Céline Huber; Chelsea Kois; Geneviève Baujat; Christopher T Gordon; Valerie Mayne; Louise Galmiche; Valérie Serre; Nicolas Goudin; Mohammed Zarhrate; Christine Bole-Feysot; Cécile Masson; Patrick Nitschké; Frans W Verheijen; Lynn Pais; Anna Pelet; Simon Sadedin; John A Pugh; Natasha Shur; Susan M White; Salima El Chehadeh; John Christodoulou; Valérie Cormier-Daire; R M W Hofstra; Stanislas Lyonnet; Tiong Yang Tan; Tania Attié-Bitach; Wilhelmina S Kerstjens-Frederikse; Jeanne Amiel; Sophie Thomas
Journal:  Am J Hum Genet       Date:  2020-05-14       Impact factor: 11.025

6.  TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human.

Authors:  Jean Marie Delalande; Nandor Nagy; Conor J McCann; Dipa Natarajan; Julie E Cooper; Gabriela Carreno; David Dora; Alison Campbell; Nicole Laurent; Polychronis Kemos; Sophie Thomas; Caroline Alby; Tania Attié-Bitach; Stanislas Lyonnet; Malcolm P Logan; Allan M Goldstein; Megan G Davey; Robert M W Hofstra; Nikhil Thapar; Alan J Burns
Journal:  Front Mol Neurosci       Date:  2021-12-23       Impact factor: 6.261

  6 in total

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