Literature DB >> 22736556

Ataxia, hyperpnoea and mental retardation: was it the molar tooth?

Osama S M Amin1, Sa'ad Seud Shwani.   

Abstract

Joubert's syndrome is a rare autosomal recessive disease, which is under-diagnosed, associated with other brain and body malformations, and carries a poor prognosis. We describe a 6-year-old boy who presented with non-progressive instability of stance and gait, mental retardation and a new onset of generalised seizures with the typical brain imaging findings of Joubert's syndrome. We believe this is the first diagnosed case of Joubert's syndrome in Iraq.

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Year:  2010        PMID: 22736556      PMCID: PMC3047379          DOI: 10.1136/bcr.10.2009.2331

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  20 in total

1.  Case 25: Joubert syndrome.

Authors:  E J van Beek; C B Majoie
Journal:  Radiology       Date:  2000-08       Impact factor: 11.105

2.  Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.

Authors:  Ian P Blair; Roxanne R Gibson; Craig L Bennett; Phillip F Chance
Journal:  Am J Med Genet       Date:  2002-01-22

3.  Follow-up in children with Joubert syndrome.

Authors:  M Steinlin; M Schmid; K Landau; E Boltshauser
Journal:  Neuropediatrics       Date:  1997-08       Impact factor: 1.947

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.  "Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation.

Authors:  B L Maria; K B Hoang; R J Tusa; A A Mancuso; L M Hamed; R G Quisling; M T Hove; E B Fennell; M Booth-Jones; D M Ringdahl; A T Yachnis; G Creel; B Frerking
Journal:  J Child Neurol       Date:  1997-10       Impact factor: 1.987

6.  Vermian agenesis without posterior fossa cyst.

Authors:  C Adamsbaum; V Moreau; C Bulteau; J Burstyn; F Lair Milan; G Kalifa
Journal:  Pediatr Radiol       Date:  1994

7.  Cerebellar vermian defects: antenatal sonographic appearance and clinical significance.

Authors:  M T Keogan; A B DeAtkine; B S Hertzberg
Journal:  J Ultrasound Med       Date:  1994-08       Impact factor: 2.153

8.  [Joubert's syndrome. Presentation of two adult siblings with favorable evolution].

Authors:  I Pascual-Castroviejo; S I Pascual-Pascual
Journal:  Neurologia       Date:  2004 Jan-Feb       Impact factor: 3.109

Review 9.  Joubert syndrome: a review.

Authors:  J M Saraiva; M Baraitser
Journal:  Am J Med Genet       Date:  1992-07-01

10.  Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.

Authors:  M D King; J Dudgeon; J B Stephenson
Journal:  Arch Dis Child       Date:  1984-08       Impact factor: 3.791

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  1 in total

1.  Sleep, Respiration and Nocturnal Paroxysmal Events in Joubert Syndrome: A Case Report.

Authors:  Rosa Peraita-Adrados
Journal:  Nat Sci Sleep       Date:  2022-08-26
  1 in total

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