Literature DB >> 25031520

Horizontal gaze palsy and scoliosis: a case report and review of the literature.

E P Samoladas1, J O'Dowd1, A Cardoso-Almeida2, A K Demetriades3.   

Abstract

BACKGROUND: The syndrome of horizontal gaze palsy with progressive scoliosis (HGPPS) is a rare human disease and while its association with scoliosis was first reported in 1974, thirty years later the responsible genetic mutations are being elucidated. This progress was due to the reporting of single interesting cases. CASE DESCRIPTION: We present the case of a 27 year-old male patient who was admitted for elective scoliosis correction surgery and who represented after an uncomplicated discharge with headache and vomiting; because of a gaze palsy he underwent brain imaging that confirmed a brainstem abnormality, consistent with the syndrome of horizontal gaze palsy with progressive scoliosis (HGPPS), a rare autosomal recessive human disease.
CONCLUSION: This rare syndrome is a good example of how single case reports can lead to advances in laboratory research and genetic characterisation of diseases, together with implications for neurodevelopment. Vigilance in the neurological examination in an otherwise 'non-neurological' scoliosis will help identify potential such cases, whilst further genetic/molecular analysis may shed further light into neuro-embryological development and patterning.

Entities:  

Keywords:  Horizontal gaze palsy; developmental biology; neurodevelopment; patterning; scoliosis

Year:  2013        PMID: 25031520      PMCID: PMC4097422     

Source DB:  PubMed          Journal:  Hippokratia        ISSN: 1108-4189            Impact factor:   0.471


  12 in total

1.  Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

Authors:  Koki Yamada; Caroline Andrews; Wai-Man Chan; Craig A McKeown; Adriano Magli; Teresa de Berardinis; Anat Loewenstein; Moshe Lazar; Michael O'Keefe; Robert Letson; Arnold London; Mark Ruttum; Naomichi Matsumoto; Nakamichi Saito; Lisa Morris; Monte Del Monte; Roger H Johnson; Eiichiro Uyama; Willem A Houtman; Berendina de Vries; Thomas J Carlow; Blaine L Hart; Nicolas Krawiecki; John Shoffner; Marlene C Vogel; James Katowitz; Scott M Goldstein; Alex V Levin; Emin C Sener; Banu T Ozturk; A Nurten Akarsu; Michael C Brodsky; Frank Hanisch; Robert P Cruse; Alina A Zubcov; Richard M Robb; Peter Roggenkäemper; Irene Gottlob; Lionel Kowal; Ravi Battu; Elias I Traboulsi; Piergiorgio Franceschini; Anna Newlin; Joseph L Demer; Elizabeth C Engle
Journal:  Nat Genet       Date:  2003-11-02       Impact factor: 38.330

2.  Intraoperative neurophysiologic discovery of uncrossed sensory and motor pathways in a patient with horizontal gaze palsy and scoliosis.

Authors:  D B MacDonald; L J Streletz; Z Al-Zayed; S Abdool; B Stigsby
Journal:  Clin Neurophysiol       Date:  2004-03       Impact factor: 3.708

3.  Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.

Authors:  T M Bosley; M A M Salih; J C Jen; D D M Lin; D Oystreck; K K Abu-Amero; D B MacDonald; Z al Zayed; H al Dhalaan; T Kansu; B Stigsby; R W Baloh
Journal:  Neurology       Date:  2005-04-12       Impact factor: 9.910

4.  Horizontal gaze palsy and progressive scoliosis due to a deleterious mutation in ROBO3.

Authors:  Khaled K Abu-Amero; Seema Kapoor; Ali Hellani; Sumit Monga; Thomas M Bosley
Journal:  Ophthalmic Genet       Date:  2011-05-19       Impact factor: 1.803

5.  Congenital scoliosis associated with encephalopathy in five children of two families.

Authors:  E K Dretakis; P N Kondoyannis
Journal:  J Bone Joint Surg Am       Date:  1974-12       Impact factor: 5.284

6.  Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Authors:  M Nakano; K Yamada; J Fain; E C Sener; C J Selleck; A H Awad; J Zwaan; P B Mullaney; T M Bosley; E C Engle
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

7.  Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations.

Authors:  Khaled K Abu-Amero; Hesham al Dhalaan; Zayed al Zayed; Ali Hellani; Thomas M Bosley
Journal:  J Neurol Sci       Date:  2008-10-01       Impact factor: 3.181

8.  Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Authors:  Joanna C Jen; Wai-Man Chan; Thomas M Bosley; Jijun Wan; Janai R Carr; Udo Rüb; David Shattuck; Georges Salamon; Lili C Kudo; Jing Ou; Doris D M Lin; Mustafa A M Salih; Tülay Kansu; Hesham Al Dhalaan; Zayed Al Zayed; David B MacDonald; Bent Stigsby; Andreas Plaitakis; Emmanuel K Dretakis; Irene Gottlob; Christina Pieh; Elias I Traboulsi; Qing Wang; Lejin Wang; Caroline Andrews; Koki Yamada; Joseph L Demer; Shaheen Karim; Jeffry R Alger; Daniel H Geschwind; Thomas Deller; Nancy L Sicotte; Stanley F Nelson; Robert W Baloh; Elizabeth C Engle
Journal:  Science       Date:  2004-04-22       Impact factor: 47.728

9.  Familial, congenital paralysis of horizontal gaze.

Authors:  R D Yee; R M Duffin; R W Baloh; S J Isenberg
Journal:  Arch Ophthalmol       Date:  1982-09

10.  Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.

Authors:  W-M Chan; E I Traboulsi; B Arthur; N Friedman; C Andrews; E C Engle
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318

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  1 in total

1.  Horizontal Gaze Palsy with Progressive Scoliosis with Overlapping Epilepsy and Learning Difficulties: A Case Report.

Authors:  Emilia Matera; Maria Giuseppina Petruzzelli; Martina Tarantini; Alessandra Gabellone; Lucia Marzulli; Romina Ficarella; Paola Orsini; Lucia Margari
Journal:  Brain Sci       Date:  2022-05-08
  1 in total

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