Arthrogryposis classification

Jump to navigation Jump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

Arthrogryposis Microchapters

Home

Overview

Classification

Pathophysiology

Causes

Epidemiology and Demographics

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Arthrogryposis classification On the Web

Most recent articles

cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Arthrogryposis classification

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Arthrogryposis classification

CDC on Arthrogryposis classification

Arthrogryposis classification in the news

Blogs on Arthrogryposis classification

Directions to Hospitals Treating Arthrogryposis

Risk calculators and risk factors for Arthrogryposis classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Classification

Some of the different types of AMC include:

  • Arthrogryposis multiplex due to muscular dystrophy.[1][2]
  • Arthrogryposis ectodermal dysplasia other anomalies, also known as Cote Adamopoulos Pantelakis syndrome, Trichooculodermovertebral syndrome, TODV syndrome and Alves syndrome.[3][4]
  • Arthrogryposis epileptic seizures migrational brain disorder.[5]
  • Arthrogryposis IUGR thoracic dystrophy,also known as Van Bervliet syndrome.[6][7]
  • Arthrogryposis like disorder, also known as Kuskokwim disease.[8]
  • Arthrogryposis-like hand anomaly and sensorineural deafness.[9][10]
  • Arthrogryposis multiplex congenita CNS calcification.[11]
  • Arthrogryposis multiplex congenita distal (AMCD)[12], with a large number of synonyms such as Arthrogryposis multiplex congenita, distal, x-linked (AMCX1)[13][14]and Arthrogryposis spinal muscular atrophy[15][16][17]
  • Gordon Syndrome, also known as Distal Arthrogryposis, Type 2A.[18]
  • Arthrogryposis multiplex congenita, distal type 2B, also known as Freeman-Sheldon syndrome variant.[19]
  • Arthrogryposis multiplex congenita neurogenic type (AMCN).[20] This particular type of AMC has been linked to the AMCN gene on locus 5q35.[21][22] Its mode of inheritance follows the Autosomal recessive patern.[23]
  • Arthrogryposis multiplex congenita pulmonary hypoplasia, also with a large number of synonyms.[24][25]
  • Arthrogryposis multiplex congenita whistling face, also known as Illum syndrome.[26][27][28][29]
  • Arthrogryposis multiplex congenita, distal type 1 (AMCD1).[30]
  • Arthrogryposis ophthalmoplegia retinopathy, also known as Oculomelic amyoplasia.[31][32][33]
  • Arthrogryposis renal dysfunction cholestasis syndrome, also known as ARC Syndrome.[34][35]

References

  1. http://pediatrics.aappublications.org/cgi/content/abstract/22/5/875
  2. Banker B, Victor M, Adams R (1957). "Arthrogryposis multiplex due to congenital muscular dystrophy". Brain. 80 (3): 319–34. PMID 13471804.
  3. Template:RareDiseases
  4. Stoll C, Alembik Y, Finck S, Janser B (1992). "Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters". Genet. Couns. 3 (1): 35–9. PMID 1590979.
  5. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1139
  6. http://www.orpha.net//consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1156
  7. Template:RareDiseases
  8. http://ctd.mdibl.org/detail.go?type=disease&acc=208200
  9. http://ctd.mdibl.org/detail.go?type=disease&acc=108200
  10. Template:RareDiseases
  11. Template:RareDiseases
  12. http://acronyms.thefreedictionary.com/Arthrogryposis+Multiplex+Congenita,+Distal
  13. http://ctd.mdibl.org/detail.go?type=disease&acc=301830
  14. http://acronyms.thefreedictionary.com/Arthrogryposis+Multiplex+Congenita,+Distal,+X-Linked
  15. Online Mendelian Inheritance in Man (OMIM) 301830
  16. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1141
  17. http://cat.inist.fr/?aModele=afficheN&cpsidt=16634238
  18. http://www.peacehealth.org/kbase/nord/nord507.htm
  19. http://www.medinet.lk/journals/CMJ/2001/december/arthrogryposis.htm
  20. http://acronyms.thefreedictionary.com/Arthrogryposis+Multiplex+Congenita,+Neurogenic+Type
  21. http://ctd.mdibl.org/detail.go?view=gene&type=disease&acc=208100
  22. http://ctd.mdibl.org/detail.go?type=disease&acc=208100
  23. Rosenmann A, Arad I (1974). "Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance". J. Med. Genet. 11 (1): 91–4. PMID 4837288.
  24. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=994
  25. Leichtman L, Say B, Barber N (1980). "Primary pulmonary hypoplasia and arthrogryposis multiplex congenita". J. Pediatr. 96 (5): 950–1. PMID 7365612.
  26. Illum N, Reske-Nielsen E, Skovby F, Askjaer S, Bernsen A (1988). "Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system". Neuropediatrics. 19 (4): 186–92. PMID 3205375.
  27. http://ctd.mdibl.org/detail.go?type=disease&acc=208155
  28. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1150
  29. Template:RareDiseases
  30. Template:RareDiseases
  31. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1154
  32. Template:RareDiseases
  33. Schrander-Stumpel C, Höweler C, Reekers A, De Smet N, Hall J, Fryns J (1993). "Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis". J. Med. Genet. 30 (1): 78–80. PMID 8423615.
  34. Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C (1995). "Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families". Eur. J. Pediatr. 154 (10): 835–9. PMID 8529684.
  35. Template:RareDiseases

Template:WH Template:WS