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1.

Osteoporosis with pseudoglioma

Osteoporosis-pseudoglioma syndrome (OPPG) is an autosomal recessive disorder characterized by severe osteoporosis and visual disturbance from childhood. Juvenile onset of osteoporosis manifests as long-bone fractures, vertebral compression fractures, kyphoscoliosis, deformity of extremities, and short stature. Congenital or early-onset visual disturbances arise from ophthalmologic problems including retinal detachment and microphthalmia (summary by Narumi et al., 2010). [from OMIM]

MedGen UID:
98480
Concept ID:
C0432252
Disease or Syndrome
2.

Absent anterior chamber of the eye

Absence of the anterior chamber of the eye owing to a developmental defect. [from HPO]

MedGen UID:
82862
Concept ID:
C0271004
Anatomical Abnormality

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