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At the age of two, he was diagnosed with craniodiaphyseal dysplasia, also known as CDD or lionitis, an extremely rare disease occurring in approximately one in every 220 million births, with fewer than 20 recorded cases. CDD is a bone disorder that causes bone tissue to build up excessively, including in the skull, causing gradual compression ...
Dec 31, 2014 · Craniodiaphyseal dysplasia (also known as CDD or lionitis) is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy.
Nov 6, 2023 · Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy.
Aug 9, 2013 · 12 Craniodiaphyseal dysplasia ICD10 Code. Craniodiaphyseal dysplasia is a very rare genetic disorder of the bone [ 1 ]. Only around 30 cases of its have been reported so far. It is also known as lionitis or simply as CDD.
An autosomal dominant or recessive form of craniotubular hyperostosis due to mutation(s) in the SOST gene, encoding sclerostin. This condition is characterized by massive generalized hyperostosis and sclerosis, especially involving the skull and facial bones, which is so severe that the resulting facial distortion is referred to as 'leontiasis ossea'; the bone deposition results in progressive ...
Nov 26, 2022 · Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy.
Craniodiaphyseal dysplasia (CDD) A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a ...
