Craniometaphyseal dysplasia, autosomal recessive type
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Craniometaphyseal dysplasia is a genetic skeletal condition characterized by overgrowth of the skull base or craniofacial bones and bone remodeling (an ongoing, lifelong process during which old bone is removed from the skeleton and new bone is added) of the metaphyses of the long bone.[1]
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The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Craniometaphyseal dysplasia, autosomal recessive type. Click on the link to go to OMIM and review these resources.
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PubMed is a searchable database of medical literature and lists journal articles that discuss Craniometaphyseal dysplasia, autosomal recessive type. Click on the link to view a sample search on this topic.
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