Literature DB >> 28213879

Arthrogryposis multiplex congenita: classification, diagnosis, perioperative care, and anesthesia.

Lulu Ma1, Xuerong Yu2.   

Abstract

Arthrogryposis multiplex congenita (AMC) is a rare disorder characterized by non-progressive, multiple contractures. In addition to affected extremities, patients may also present microstomia, decreased temporomandibular joint mobility. Although the etiology of AMC is unclear, any factor that decreases fetal movement is responsible for AMC. Thus, accurate diagnosis and classification are crucial to the appropriate treatment of AMC. The development of ultrasound technology has enabled prenatal diagnosis. Very early treatment is favorable, and multidisciplinary treatment is necessary to improve the function of AMC patients. Most patients require surgery to release contracture and reconstruct joints. However, perioperative care is challenging, and difficult airway is the first concern of anesthesiologists. Postoperative pulmonary complications are common and regional anesthesia is recommended for postoperative analgesia. This review on AMC is intended for anesthesiologists. Thus, we discuss the treatment and perioperative management of patients undergoing surgery, as well as the diagnosis and classification of AMC.

Entities:  

Keywords:  amyoplasia; anesthesia; arthrogryposis; distal arthrogryposis

Mesh:

Year:  2017        PMID: 28213879     DOI: 10.1007/s11684-017-0500-4

Source DB:  PubMed          Journal:  Front Med        ISSN: 2095-0217            Impact factor:   4.592


  48 in total

Review 1.  Teratogen update: maternal myasthenia gravis as a cause of congenital arthrogryposis.

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Journal:  Teratology       Date:  2000-11

Review 2.  EUROCAT: 25 years of European surveillance of congenital anomalies.

Authors:  H Dolk
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2005-09       Impact factor: 5.747

3.  Anesthesia for Freeman-Sheldon syndrome using a folded laryngeal mask airway.

Authors:  Albert Chen; Hsien-Yong Lai; Yi Lee; Yao-Lin Yang; Jyu-Shiou Ho; Ming-Hwang Shyr
Journal:  Anesth Analg       Date:  2005-08       Impact factor: 5.108

4.  Multiple congenital contractures: birth prevalence, etiology, and outcome.

Authors:  Niklas Darin; Eva Kimber; Anna-Karin Kroksmark; Már Tulinius
Journal:  J Pediatr       Date:  2002-01       Impact factor: 4.406

5.  Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1.

Authors:  Christina A Gurnett; David M Desruisseau; Kevin McCall; Ryan Choi; Zachary I Meyer; Michael Talerico; Sara E Miller; Jeong-Sun Ju; Alan Pestronk; Anne M Connolly; Todd E Druley; Conrad C Weihl; Mathew B Dobbs
Journal:  Hum Mol Genet       Date:  2010-01-02       Impact factor: 6.150

6.  Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population.

Authors:  O B Navti; E Kinning; P Vasudevan; M Barrow; H Porter; E Howarth; J Konje; M Khare
Journal:  Prenat Diagn       Date:  2010-01       Impact factor: 3.050

Review 7.  Freeman Sheldon syndrome: severe upper airway obstruction requiring neonatal tracheostomy.

Authors:  P J Robinson
Journal:  Pediatr Pulmonol       Date:  1997-06

8.  Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin.

Authors:  Yavuz Bayram; Ender Karaca; Zeynep Coban Akdemir; Elif Ozdamar Yilmaz; Gulsen Akay Tayfun; Hatip Aydin; Deniz Torun; Sevcan Tug Bozdogan; Alper Gezdirici; Sedat Isikay; Mehmed M Atik; Tomasz Gambin; Tamar Harel; Ayman W El-Hattab; Wu-Lin Charng; Davut Pehlivan; Shalini N Jhangiani; Donna M Muzny; Ali Karaman; Tamer Celik; Ozge Ozalp Yuregir; Timur Yildirim; Ilhan A Bayhan; Eric Boerwinkle; Richard A Gibbs; Nursel Elcioglu; Beyhan Tuysuz; James R Lupski
Journal:  J Clin Invest       Date:  2016-01-11       Impact factor: 14.808

9.  Functional upper airway obstruction in a child with Freeman-Sheldon syndrome.

Authors:  Joerg Schefels; Tobias G Wenzl; Ulrich Merz; Vincent Ramaekers; Josef Holzki; Sabine Rudnik-Schoeneborn; Benita Hermanns; Helmut Hörnchen
Journal:  ORL J Otorhinolaryngol Relat Spec       Date:  2002 Jan-Feb       Impact factor: 1.538

10.  Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.

Authors:  Dan Mejlachowicz; Flora Nolent; Jérome Maluenda; Hanitra Ranjatoelina-Randrianaivo; Fabienne Giuliano; Ivo Gut; Damien Sternberg; Annie Laquerrière; Judith Melki
Journal:  Am J Hum Genet       Date:  2015-09-10       Impact factor: 11.025

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  5 in total

Review 1.  Skeletal myosin binding protein-C: An increasingly important regulator of striated muscle physiology.

Authors:  James W McNamara; Sakthivel Sadayappan
Journal:  Arch Biochem Biophys       Date:  2018-10-17       Impact factor: 4.013

Review 2.  The Prognosis of Arthrofibroses: Prevalence, Clinical Shortcomings, and Future Prospects.

Authors:  William A Blessing; Amanda K Williamson; Jack R Kirsch; Mark W Grinstaff
Journal:  Trends Pharmacol Sci       Date:  2021-03-29       Impact factor: 14.819

3.  Early open reduction of dislocated hips using a modified Smith-Petersen approach in arthrogyposis multiplex congenita.

Authors:  Mingyuan Miao; Haiqing Cai; Zhigang Wang; Liwei Hu; Jingxia Bian; Haoqi Cai
Journal:  BMC Musculoskelet Disord       Date:  2020-03-04       Impact factor: 2.362

4.  Case Report: A de novo Variant in NALCN Associated With CLIFAHDD Syndrome in a Chinese Infant.

Authors:  Zhenyu Liao; Yali Liu; Yimin Wang; Qin Lu; Yu Peng; Qingsong Liu
Journal:  Front Pediatr       Date:  2022-07-13       Impact factor: 3.569

Review 5.  Difficult airway management in children and young adults with arthrogryposis.

Authors:  Glenn Isaacson; Elizabeth T Drum
Journal:  World J Otorhinolaryngol Head Neck Surg       Date:  2018-07-13
  5 in total

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