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Dictionary » Trimethadione embryopathy
 

Trimethadione embryopathy

Introduction: Trimethadione embryopathy

Description of Trimethadione embryopathy

Trimethadione embryopathy (medical condition): A rare disorder caused by fetal exposure to trimethadione (anticonvulsant drug) and resulting in various physical and developemental abnormalities.

See also:

German syndrome:
  »Introduction: German syndrome
  »Symptoms of German syndrome

Trimethadione embryopathy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Trimethadione embryopathy:

Trimethadione embryopathy: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Trimethadione embryopathy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Trimethadione embryopathy, or a subtype of Trimethadione embryopathy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Trimethadione embryopathy as a Disease

Trimethadione embryopathy: Another name for German syndrome (or close medical condition association).
  »Introduction: German syndrome
  »Symptoms of German syndrome

Symptoms of Trimethadione embryopathy (German syndrome)

Some of the symptoms of Trimethadione embryopathy incude:

See full list of 29 symptoms of Trimethadione embryopathy (German syndrome)

Trimethadione embryopathy: Related Disease Topics

These medical disease topics may be related to Trimethadione embryopathy:

Terms associated with Trimethadione embryopathy:

Terms Similar to Trimethadione embryopathy:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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