OI congenital

Introduction: OI congenital

Description of OI congenital

OI congenital (medical condition): A rare lethal form of a genetic connective tissue disorder characterized...more »

See also:

Osteogenesis imperfecta, type 2A:
  »Introduction: Osteogenesis imperfecta, type 2A
  »Symptoms of Osteogenesis imperfecta, type 2A

OI congenital: Related Topics

These medical condition or symptom topics may be relevant to medical information for OI congenital:

• Congenital
• Congenital disease
• Congenital disorder

OI congenital as a Disease

OI congenital: Another name for Osteogenesis imperfecta, type 2A (or close medical condition association).
  »Introduction: Osteogenesis imperfecta, type 2A
  »Symptoms of Osteogenesis imperfecta, type 2A

OI congenital: Related Diseases

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

• Genetic conditions
• Musculoskeletal conditions
• Bone or skeletal conditions
• Growth conditions
• Connective tissue conditions
• Respiratory conditions
• Congenital conditions

Symptoms of OI congenital (Osteogenesis imperfecta, type 2A)

Some of the symptoms of OI congenital incude:

• Large head
• Underdeveloped dentin
• Underdeveloped pulp
• Soft cranium
• Membranous cranium

See full list of 42 symptoms of OI congenital (Osteogenesis imperfecta, type 2A)

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