CDAGS syndrome

Introduction: CDAGS syndrome

Description of CDAGS syndrome

CDAGS syndrome (medical condition): A very rare disorder characterized primarily by the premature fusion of skull bones (coronal sutures), anal anomalies and a skin disorder called porokeratosis.

See also:

Craniosynostosis, anal anomalies, and porokeratosis:
  »Introduction: Craniosynostosis, anal anomalies, and porokeratosis
  »Symptoms of Craniosynostosis, anal anomalies, and porokeratosis

CDAGS syndrome: Rare Disease

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

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

CDAGS syndrome as a Disease

CDAGS syndrome: Another name for Craniosynostosis, anal anomalies, and porokeratosis (or close medical condition association).
  »Introduction: Craniosynostosis, anal anomalies, and porokeratosis
  »Symptoms of Craniosynostosis, anal anomalies, and porokeratosis

Symptoms of CDAGS syndrome (Craniosynostosis, anal anomalies, and porokeratosis)

Some of the symptoms of CDAGS syndrome incude:

• Abnormal skull shape
• Abnormal anal position
• Imperforate anus
• Genitourinary malformation
• Skin eruption

See full list of 12 symptoms of CDAGS syndrome (Craniosynostosis, anal anomalies, and porokeratosis)

CDAGS syndrome: Related Disease Topics

These medical disease topics may be related to CDAGS syndrome:

• rare disorder
• porokeratosis

Terms associated with CDAGS syndrome:

Terms Similar to CDAGS syndrome:

• Craniosynostosis and clavicular hypoplasia, Delayed closure of the fontanel, Anal anomalies and Genitourinary malformations
• Craniosynostosis, anal anomalies, and porokeratosis
• CAP syndrome

Source - NIH

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Medical dictionaries:

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More Medical Dictionary Topics

Type 4 Achondrogenesis

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