Literature DB >> 17534630

Chiari I malformation and idiopathic growth hormone deficiency in siblings: report of three cases.

R Lee Murphy1, R Shane Tubbs, Paul A Grabb, W Jerry Oakes.   

Abstract

INTRODUCTION: The authors report a case of three brothers. CASE DESCRIPTIONS: Two of these siblings presented with congenital growth hormone deficiency (GHD) and Chiari I malformation (CIM). The third younger brother has been found not to have GHD or the CIM. DISCUSSION: Sparse cases of these two clinical occurrences have been reported. Further, the posterior cranial fossa (PF) has been determined to be altered in patients with CIM and GHD.
CONCLUSION: Our current case reports strengthen the association between these two pathological entities and, to our knowledge, is the first description of both defects in siblings.

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Year:  2007        PMID: 17534630     DOI: 10.1007/s00381-007-0374-x

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  15 in total

1.  Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.

Authors:  T H Milhorat; M W Chou; E M Trinidad; R W Kula; M Mandell; C Wolpert; M C Speer
Journal:  Neurosurgery       Date:  1999-05       Impact factor: 4.654

Review 2.  History, anatomic forms, and pathogenesis of Chiari I malformations.

Authors:  Edgardo Schijman
Journal:  Childs Nerv Syst       Date:  2004-02-05       Impact factor: 1.475

3.  Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: case report.

Authors:  J L Atkinson; E Kokmen; G M Miller
Journal:  Neurosurgery       Date:  1998-02       Impact factor: 4.654

4.  Morphogenesis of experimentally induced Arnold--Chiari malformation.

Authors:  M Marin-Padilla; T M Marin-Padilla
Journal:  J Neurol Sci       Date:  1981-04       Impact factor: 3.181

5.  [Cerebral anomalies associated with growth hormone insufficiency in children: major markers for diagnosis?].

Authors:  N Arifa; J Léger; C Garel; P Czernichow; M Hassan
Journal:  Arch Pediatr       Date:  1999-01       Impact factor: 1.180

6.  MR imaging in idiopathic growth hormone deficiency.

Authors:  J Hamilton; S Blaser; D Daneman
Journal:  AJNR Am J Neuroradiol       Date:  1998-10       Impact factor: 3.825

Review 7.  Familial syringomyelia: the first Japanese case and review of the literature.

Authors:  Ichiro Yabe; Seiji Kikuchi; Kunio Tashiro
Journal:  Clin Neurol Neurosurg       Date:  2002-12       Impact factor: 1.876

8.  Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa.

Authors:  R Shane Tubbs; John C Wellons; Matthew D Smyth; Alfred A Bartolucci; Jeffrey P Blount; W Jerry Oakes; Paul A Grabb
Journal:  Pediatr Neurosurg       Date:  2003-06       Impact factor: 1.162

9.  Surgical experience in 130 pediatric patients with Chiari I malformations.

Authors:  R Shane Tubbs; Matthew J McGirt; W Jerry Oakes
Journal:  J Neurosurg       Date:  2003-08       Impact factor: 5.115

Review 10.  Familial syringomyelia: case report and review of the literature.

Authors:  A Zakeri; F E Glasauer; J G Egnatchik
Journal:  Surg Neurol       Date:  1995-07
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  4 in total

1.  Development of profound Chiari I malformation and cerebellar tissue loss and resolution following shunting of posterior fossa extra-axial cyst. Case report.

Authors:  Rabia Khan; Peter Oakes; R Shane Tubbs; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2016-07-21       Impact factor: 1.475

2.  Chiari type 1 anomaly in pseudohypoparathyroidism type Ia: pathogenetic hypothesis.

Authors:  Juan F Martínez-Lage; Encarna Guillén-Navarro; Antonio L López-Guerrero; María José Almagro; Beatriz Cuartero-Pérez; Pedro de la Rosa
Journal:  Childs Nerv Syst       Date:  2011-10-13       Impact factor: 1.475

3.  Evolution of tonsillar ectopia associated with frontal encephalocoele.

Authors:  Dharmendra Ganesan; Richard D Hayward; Dominic N Thompson
Journal:  Childs Nerv Syst       Date:  2009-02-24       Impact factor: 1.475

4.  Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Authors:  Christina A Markunas; Karen Soldano; Kaitlyn Dunlap; Heidi Cope; Edgar Asiimwe; Jeffrey Stajich; David Enterline; Gerald Grant; Herbert Fuchs; Simon G Gregory; Allison E Ashley-Koch
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240

  4 in total

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