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Fetal trimethadione syndrome

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Fetal trimethadione syndrome
Other namesGerman syndrome
Trimethadione.svg
Condition is caused by Trimethadione (and paramethadione)

Fetal trimethadione syndrome (also known as paramethadione syndrome, German syndrome, tridione syndrome, among others[1]) is a set of birth defects caused by the administration of the anticonvulsants trimethadione (also known as Tridione) or paramethadione to epileptic mothers during pregnancy.[2]

Fetal trimethadione syndrome is classified as a rare disease by the National Institute of Health's Office of Rare Diseases,[3] meaning it affects less than 200,000 individuals in the United States.[4]

The fetal loss rate while using trimethadione has been reported to be as high as 87%.[5]

Presentation[]

Fetal trimethadione syndrome is characterized by the following major symptoms as a result of the teratogenic characteristics of trimethadione.[2][6]

  • Cranial and facial abnormalities which include; microcephaly, flattening, V-shaped eyebrows and a short nose
  • Cardiovascular abnormalities
  • Absent kidney and ureter
  • Meningocele, a birth defect of the spine
  • Omphalocele, a birth defect where portions of the abdominal contents project into the umbilical cord
  • A delay in mental and physical development
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Diagnosis[]

Treatment[]

References[]

  1. ^ Additional names include trimethadione embryopathy and trimethadione syndrome.
  2. ^ Jump up to: a b Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes - Retrieved January 2007
  3. ^ Fetal trimethadione syndrome on the ORD website. Retrieved January 2007
  4. ^ NIH's Office of Rare Diseases Archived 2009-02-06 at the Wayback Machine Retrieved January 2007
  5. ^ Teratology and Drug Use During Pregnancy Retrieved January 2007
  6. ^ The fetal trimethadione syndrome: report of an additional family and further delineation of this syndrome Retrieved January 2007

External links[]

Classification
External resources
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