May Be Caused by

Adenosine deaminase deficiency with severe combined immunodeficiency and chondro-osseous dysplasia

Battered child syndrome

Bisphosphonate therapy

Brachyolmia

Chronic recurrent multifocal osteomyelitis

Craniometadiaphyseal dysplasia Wormian bone type

Deferoxamine-induced skeletal dysplasia

Dyggve-Melchior-Clausen dysplasia

Dysosteosclerosis

Erdheim-Chester disease

Fetal hypermagnesemia syndrome

Hardcastle syndrome

Hypercalcemia

Hyperparathyroidism

Hypervitaminosis D

Hypochondrogenesis

Hypoparathyroidism

Idiopathic symptomatic metaphyseal sclerosis in children

Lead intoxication

Leukemia

Metaphyseal chondrodysplasia

Metaphyseal chondrodysplasia anadysplasia type

Metaphyseal chondrodysplasia Jansen type

Metaphyseal chondrodysplasia McKusick type

Metaphyseal chondrodysplasia Schmid type

Metaphyseal-sella turcica dysplasia Rosenberg type

Metastasis

Microcephalic osteodysplastic dysplasia

Neoplasm

Osteosclerotic metaphyseal dysplasia

Pacman dysplasia

Plasma-cell osteomyelitis

Pseudoachondroplasia

Round distal femoral epiphyseal micromelic dysplasia

Saldino-Mainzer syndrome

Schneckenbecken dysplasia

Shwachman–Diamond syndrome

Spondyloepimetaphyseal dysplasia

Spondyloepimetaphyseal dysplasia dominant metatropic type

Spondyloepimetaphyseal dysplasia Irapa type

Spondyloepimetaphyseal dysplasia Iraqi type

Spondyloepimetaphyseal dysplasia leptodactylic type

Spondyloepimetaphyseal dysplasia short limb-hand-abnormal calcification type

Spondyloepimetaphyseal dysplasia Strudwick type

Spondyloepimetaphyseal dysplasia with joint laxity

Spondylomegaepiphyseal-metaphyseal dysplasia

Spondylometaphyseal dysplasia

Spondylometaphyseal dysplasia Kozlowski type

Spondylometaphyseal dysplasia Sedaghatian type