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SUDDEN INFANT DEATH SYNDROME

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Description

Sudden infant death syndrome (SIDS) is a diagnosis of exclusion which should be made only after a thorough autopsy without identification of a specific cause of death (Mage and Donner, 2004). Weese-Mayer et al. (2007) provided a detailed review of genetic factors that have been implicated in SIDS. The authors concluded that SIDS represents more than 1 entity and has a heterogeneous etiology most likely involving several different genetically controlled metabolic pathways.

OMIM

  • Mode of Inheritance

  • Multifactorial inheritance
  • Autosomal recessive inheritance

VARIANTS

59

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Genes

External Links

  • OMIM

    272120

  • Orphanet
  • HPO
  • Medgen

    C0038644

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