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ACS3

Introduction: ACS3

Description of ACS3

ACS3 (medical condition): A rare genetic disorder characterized by premature joining...more »

See also:

Saethre-Chotzen Syndrome:
  »Introduction: Saethre-Chotzen Syndrome
  »Symptoms of Saethre-Chotzen Syndrome

ACS3: Rare Disease

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

ACS3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ACS3, or a subtype of ACS3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ACS3 as a Disease

ACS3: Another name for Saethre-Chotzen Syndrome (or close medical condition association).
  »Introduction: Saethre-Chotzen Syndrome
  »Symptoms of Saethre-Chotzen Syndrome

ACS3: Related Diseases

ACS3: ACS3 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of ACS3 (Saethre-Chotzen Syndrome)

Some of the symptoms of ACS3 incude:

  • Premature closing of coronal sutures
  • Premature closing of lambdoid sutures
  • Abnormal cranial development
  • Premature closing of skull bones
  • Premature closing of metopic sutures

ACS3: Related Disease Topics

These medical disease topics may be related to ACS3:

Terms associated with ACS3:

Terms Similar to ACS3:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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