Vrolik Disease (Type II)

It is possible that the major title of the record Osteogenesis Imperfecta is not the name you anticipated. Please check the synonyms specifying to discover the alternating name(s) and disorder neighborhood(s) covered by this record.


  • Breakable Bone Condition
  • Ekman-Lobstein Condition
  • Lobstein Condition (Type I)
  • OI
  • Vrolik Condition (Kind II)

Condition Neighborhoods

  • Osteogenesis Imperfecta Type I
  • Osteogenesis Imperfecta Type II
  • Osteogenesis Imperfecta Type III
  • Osteogenesis Imperfecta Type IV

General Conversation
Osteogenesis Imperfecta (OI) is a team of rare disorders impacting the connective cells and identified by extremely delicate bones that damage or fracture conveniently (breakable bones), commonly without apparent reason. The certain signs and symptoms as well as physical findings related to OI differ greatly from situation to situation. The intensity of OI likewise differs substantially, also amongst people of the very same family members. OI may be a light problem or could cause serious problems. Four major types of OI have been recognized. OI kind I is one of the most usual and the mildest form of the condition. OI kind II is the most serious. In many cases, the numerous types of osteogenesis imperfecta are inherited as autosomal leading traits.

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