Literature DB >> 26561226

Chiari malformation, syringomyelia and bulbar palsy in X linked hypophosphataemia.

Laura Watts1, Paul Wordsworth2.   

Abstract

X linked hypophosphataemia (XLH) is a rare condition with numerous musculoskeletal complications. It may mimic other more familiar conditions, such as vitamin D deficiency, ankylosing spondylitis or diffuse idiopathic skeletal hyperostosis. We describe two cases with Chiari type 1 malformations and syringomyelia, neither of which is well recognised in XLH. The first presented late with the additional complications of spinal cord compression, pseudofracture, renal stones and gross femoroacetabular impingement requiring hip replacement. The second also had bulbar palsy; the first case to be described in this condition, to the best of our knowledge. We wish to raise awareness of the important neurological complications of syringomyelia, Chiari malformation, spinal cord compression and bulbar palsy when treating these patients. We also wish to draw attention to the utility of family history and genetic testing when making the diagnosis of this rare but potentially treatable condition. 2015 BMJ Publishing Group Ltd.

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Mesh:

Year:  2015        PMID: 26561226      PMCID: PMC4654153          DOI: 10.1136/bcr-2015-211961

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


  12 in total

1.  X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults.

Authors:  I R Reid; D C Hardy; W A Murphy; S L Teitelbaum; M A Bergfeld; M P Whyte
Journal:  Medicine (Baltimore)       Date:  1989-11       Impact factor: 1.889

2.  Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia.

Authors:  Thomas O Carpenter; Erik A Imel; Mary D Ruppe; Thomas J Weber; Mark A Klausner; Margaret M Wooddell; Tetsuyoshi Kawakami; Takahiro Ito; Xiaoping Zhang; Jeffrey Humphrey; Karl L Insogna; Munro Peacock
Journal:  J Clin Invest       Date:  2014-02-24       Impact factor: 14.808

3.  Chiari I malformation: association with hypophosphatemic rickets and MR imaging appearance.

Authors:  K S Caldemeyer; J C Boaz; R S Wappner; C C Moran; R R Smith; J P Quets
Journal:  Radiology       Date:  1995-06       Impact factor: 11.105

Review 4.  The changing face of hypophosphatemic disorders in the FGF-23 era.

Authors:  Janet Y Lee; Erik A Imel
Journal:  Pediatr Endocrinol Rev       Date:  2013-06

5.  Pediatric and adult Chiari malformation Type I surgical series 1965-2013: a review of demographics, operative treatment, and outcomes.

Authors:  Aska Arnautovic; Bruno Splavski; Frederick A Boop; Kenan I Arnautovic
Journal:  J Neurosurg Pediatr       Date:  2014-12-05       Impact factor: 2.375

6.  Prolonged Correction of Serum Phosphorus in Adults With X-Linked Hypophosphatemia Using Monthly Doses of KRN23.

Authors:  Erik A Imel; Xiaoping Zhang; Mary D Ruppe; Thomas J Weber; Mark A Klausner; Takahiro Ito; Maria Vergeire; Jeffrey S Humphrey; Francis H Glorieux; Anthony A Portale; Karl Insogna; Munro Peacock; Thomas O Carpenter
Journal:  J Clin Endocrinol Metab       Date:  2015-04-28       Impact factor: 5.958

7.  A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium.

Authors: 
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

8.  Hip and knee arthroplasty in hypophosphatemic rickets.

Authors:  A Noelle Larson; Robert T Trousdale; Mark W Pagnano; Arlen D Hanssen; David G Lewallen; Joaquin Sanchez-Sotelo
Journal:  J Arthroplasty       Date:  2009-08-12       Impact factor: 4.757

Review 9.  Cervical spinal cord compression attributable to a calcified intervertebral disc in a patient with X-linked hypophosphatemic rickets: case report and review of the literature.

Authors:  Martin Soehle; Adrian T H Casey
Journal:  Neurosurgery       Date:  2002-07       Impact factor: 4.654

10.  Sagittal synostosis in X-linked hypophosphatemic rickets and related diseases.

Authors:  Guido Currarino
Journal:  Pediatr Radiol       Date:  2007-06-06
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  4 in total

1.  Digenic mutations of human OCRL paralogs in Dent's disease type 2 associated with Chiari I malformation.

Authors:  Daniel Duran; Sheng Chih Jin; Tyrone DeSpenza; Carol Nelson-Williams; Andrea G Cogal; Elizabeth W Abrash; Peter C Harris; John C Lieske; Serena Je Shimshak; Shrikant Mane; Kaya Bilguvar; Michael L DiLuna; Murat Günel; Richard P Lifton; Kristopher T Kahle
Journal:  Hum Genome Var       Date:  2016-12-08

2.  Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study.

Authors:  Takuo Kubota; Seiji Fukumoto; Hae Il Cheong; Toshimi Michigami; Noriyuki Namba; Nobuaki Ito; Shin Tokunaga; Yoshimi Gibbs; Keiichi Ozono
Journal:  BMJ Open       Date:  2020-06-29       Impact factor: 2.692

3.  Burden of disease associated with X-linked hypophosphataemia in adults: a systematic literature review.

Authors:  L Seefried; M Smyth; R Keen; P Harvengt
Journal:  Osteoporos Int       Date:  2020-07-24       Impact factor: 4.507

Review 4.  X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management.

Authors:  Giampiero Igli Baroncelli; Stefano Mora
Journal:  Front Endocrinol (Lausanne)       Date:  2021-08-06       Impact factor: 5.555

  4 in total

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