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

Images courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

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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