Dyschondroplasia
Dyschondroplasia | |
Dyschondroplasia: Gross whole body viewed anterior infant female with dyschondroplasia Image courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology | |
ICD-9 | 756.4 |
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Dyschondroplasia is a rare genetic disorder characterized by abnormal bone development.
Etiology is unknown.
Signs
- Genu valgum
- Unilateral joint deformity
- Knobby fingers
Diagnosis
Plain X-Ray
- Dilated bone cortex
- Rarefied shaft with streaks
- Translucent metaphysis
- Bones shortened
Pathological Findings
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Dyschondroplasia: Gross whole body viewed anterior infant female with dyschondroplasia
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Dyschondroplasia: Gross whole body viewed from rear an infant with dyschondroplasia