SHOX gene deletions have been identified as the major cause of Leri–Weill syndrome.[3]
Leri–Weill dyschondrosteosis is characterized by
mesomelic short stature, with bowing of the
radius more so than the
ulna in the forearms and bowing of the
tibia while sparing the
fibula.[citation needed]
Diagnosis
Diagnosis is made following genetic blood testing.[citation needed]
Treatment
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^Léri A, Weill JA (1929). "Une affection congénitale et symétrique du développement osseux. La dyschondrostéose". Bulletins et Mémoires de la Société Médicale des Hôpitaux de Paris. 53: 1491–1494.