Regressive spondylometaphyseal dysplasia

Orpha code: 448267OMIM code: 618019

Definicja

Regressive spondylometaphyseal dysplasia is a rare, primary bone dysplasia characterized by mild short stature, rhizomelic shortening of the arms and legs, bowing of long bones with widened and irregular metaphyses, thoracolumbar kyphosis, and metacarpal shortening. A marked improvement of the radiologic skeletal features is typical. Pelger-Huet anomaly (i.e. dumbbell shape bilobed nuclei of neutrophils) is a characteristic hematological feature of this disease.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
448267
Kod OMIM
618019
Kod ICD10
Q77.8
Kod ICD11
-

No additional description.

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