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Congenital toxoplasmosis

Disease definition

A rare fetopathy characterized by ocular, visceral or intracranial lesions secondary to maternal primary infection by Toxoplasma gondii (Tg).

ORPHA:858

Classification level: Disorder
  • Synonym(s):
    • Mother-to-child transmission of toxoplasmosis
    • Toxoplasma embryofetopathy
    • Toxoplasma embryopathy
  • Prevalence: Unknown
  • Inheritance: Not applicable 
  • Age of onset: Antenatal, Neonatal, Infancy
  • ICD-10: P37.1
  • OMIM: -
  • UMLS: C0040560
  • MeSH: D014125
  • GARD: -
  • MedDRA: 10010652

Detailed information

Professionals

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.