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Sheldon-hall syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Sheldon-Hall syndrome (SHS) is a rare multiple congenital contracture syndrome characterized by contractures of the distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate.

Synonyms

  • DA2B
  • Freeman Sheldon syndrome, variant
  • Freeman Sheldon variant
  • Freeman-Sheldon syndrome variant
  • Sheldon-Hall syndrome
  • arthrogryposis multiplex congenita distal type 2B
  • arthrogryposis multiplex congenita distal type II with craniofacial abnormalities
  • arthrogryposis multiplex congenita, distal, type 2B
  • arthrogryposis multiplex congenita, distal, type II, with craniofacial abnormalities
  • arthrogryposis, distal, type 2B
  • distal arthrogryposis type 2B
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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