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Dictionary » Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia
 

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia

Introduction: Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia

Description of Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia (medical condition): A rare progressive congenital syndrome involving degeneration of the...more »

See also:

Pena-Shokeir syndrome Type 2:
  »Introduction: Pena-Shokeir syndrome Type 2
  »Symptoms of Pena-Shokeir syndrome Type 2

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia:

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Rare Disease

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

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia, or a subtype of Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia as a Disease

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Another name for Pena-Shokeir syndrome Type 2 (or close medical condition association).
  »Introduction: Pena-Shokeir syndrome Type 2
  »Symptoms of Pena-Shokeir syndrome Type 2

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Related Diseases

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia (Pena-Shokeir syndrome Type 2)

Some of the symptoms of Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia incude:

  • Reduced white matter of brain
  • Gray mottling of white matter of brain
  • Subependymal focal gliosis of third brain ventricle
  • Focal microgyria
  • Hypoplasia of temporal and hippocampal gyri

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: Related Disease Topics

These medical disease topics may be related to Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia:

Terms associated with Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia:

Terms Similar to Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia:

Source - NIH

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