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Meckel Syndrome

Abstract

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Synonyms of Meckel Syndrome

  • Dysencephalia Splanchnocystica
  • Gruber Syndrome
  • Meckel-Gruber Syndrome
  • MES
  • MKS

Disorder Subdivisions

  • Meckel Syndrome Type 1
  • Meckel Syndrome Type 2
  • Meckel Syndrome Type 3

General Discussion

Meckel syndrome is a rare inherited disorder characterized by abnormalities affecting several organ systems of the body (multisystem). Three classic symptoms are normally associated with Meckel syndrome: protrusion of a portion of the brain and its surrounding membranes (meninges) through a defect in the back or front of the skull (occipital encephalocele), multiple cysts on the kidneys (polycystic kidneys), and extra fingers and/or toes (polydactyly). Affected children may also have abnormalities affecting the head and face (craniofacial area), liver, lungs, and genitourinary tract. Meckel syndrome is inherited as an autosomal recessive trait.

Organizations related to Meckel Syndrome

Please note that some of these organizations may provide information concerning certain conditions potentially associated with this disorder.

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