Down syndrome: Difference between revisions

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===Orthopedic===
===Orthopedic===
*Cervical spine - increased risk of [[atlanto-occipital dissociation]]
*Cervical spine - increased risk of [[atlanto-occipital dissociation]]
*Ligamentous laxity increases the risk of dislocation or subluxation at any joint
*Ligamentous laxity increases the risk of [[joint dislocations|dislocation]] or subluxation at any joint


==Evaluation==
==Evaluation==

Revision as of 18:52, 28 September 2019

Background

  • Caused by trisomy 21, the most common chromosomal disorder in humans
  • Patients are at increased risk for injuries and diseases related to issues caused by their genetic condition.

Clinical Features

All patients have intellectual disability. Patients may also have some or all of the following abnormalities:

  • Mental impairment
  • Abnormal teeth
  • Stunted growth
  • Slanted eyes
  • Umbilical hernia
  • Shortened hands
  • Increased skin at the back of the neck
  • Short neck
  • Hypotonia
  • Obstructive sleep apnea
  • Ligamentous laxity
  • Single transverse palmar crease (Simian crease)
  • Large tongue
  • Congenital heart disease
  • Flattened nose
  • Strabismus
  • Undescended testicles

Pathology by System

Patients with Down syndrome may have some or all of the following EM-relevant pathologies

Airway/Respiratory

Cardiac

Endocrine

Gastrointestinal

HEENT

  • Increased incidence of cataracts, hearing loss
  • Small ear canals with increased rates of otitis media
  • Early onset hearing loss.

Orthopedic

Evaluation

  • Evaluation and management should focus on the patient's complaint or anatomic area of of concern while taking into consideration the above disease specific pathologies.

Management

  • Based on diagnosis and specific underlying problem

Disposition

  • Based on specific underlying problem

See Also

Cervical injury (peds)

Video

{{#widget:YouTube|id=M9jfoCA8paA}}

References