Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita

✍ Scribed by Unger, Sheila ;Korkko, Jarmo ;Krakow, Deborah ;Lachman, Ralph S. ;Rimoin, David L. ;Cohn, Daniel H.

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 225 KB
• Volume: 104
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.10062

✦ Synopsis

Pseudoachondroplasia (PSACH) and spondyloepiphyseal dysplasia congenita (SEDC) are autosomal dominant forms of short-limb short stature caused by mutations in genes that encode structural components of the cartilage extracellular matrix. PSACH results from mutations in the cartilage oligomeric matrix protein (COMP) gene, while SEDC is caused by mutations in the gene for type II procollagen (COL2A1). We report a child with a distinct skeletal dysplasia due to the combined phenotypes of PSACH and SEDC. The proband's mother had PSACH and his father had SEDC. The child was suspected of having both phenotypes on the basis of the severity of his clinical and radiographic ®ndings, and this was con-®rmed by molecular analysis. The COMP gene mutation (C348R), while not previously published, is typical of those in PSACH patients, whereas the COL2A1 mutation (T1370M) is somewhat atypical, as it predicts an amino acid change within the carboxyl-terminal region of the protein.

Both mutations segregated with their respective phenotypes within this family. The description and natural history of the double heterozygote phenotype may be useful in counseling families regarding risk and prognosis.