Osteogenesis imperfecta | Medibuddy
26th February 2025

Osteogenesis imperfecta

Osteogenesis imperfecta is a heritable connective tissue disorder caused by type 1 collagen abnormalities, either decreased production or disrupted structure or processing.

Classification of osteogenesis imperfecta

Originally, four subtypes were described, and these are most commonly asked about in MRCP, although the disease is now felt to be a spectrum, and other subgroups have been added. Types I and IV encompass 90% of patients.

Type Genetics Sclera Features
Type I Autosomal dominant

Quantitative defect

Blue Least severe

Fractures when start walking

Hearing loss 50%

Type II Autosomal recessive

Qualitative defect

Blue Die in utero or early infancy
Type III Autosomal recessive

Qualitative defect

Normal Most severe survivable form

Fractures at birth

Type IV Autosomal dominant

Qualitative defect

Normal Moderate severity

Bowing bones and vertebral fractures

Hearing normal

Table 7 Clinical features and heritability of osteogenesis imperfecta types I to IV

Clinical features of osteogenesis imperfecta

Other suggestive features include short stature, scoliosis, easy bruising, increased skin laxity and dental abnormalities. Very mild disease can present as premature osteoporosis, particularly postpartum, or accelerated osteoporosis following menopause.

Management is supportive, including physiotherapy, targeted surgical intervention as required, and screening for osteoporosis.

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