Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43.

Abstract

Oculo-dento-digital dysplasia (ODDD, OMIM no.164210) is a pleiotropic disorder caused by mutations in the GJA1 gene that codes for the gap junction protein connexin 43. While the gene is highly expressed in skin, ODDD is usually not associated with skin symptoms. We recently described a family with ODDD and palmoplantar keratoderma. Interestingly, mutation carriers had a novel dinucleotide deletion in the GJA1 gene that resulted in truncation of part of the C-terminus. We speculated, that truncation of the C-terminus may be uniquely associated with skin disease in ODDD. Here, we describe a patient with ODDD and palmar hyperkeratosis caused by a novel dinucleotide deletion that truncates most of the connexin 43 C-terminus. Thus, our findings support the notion that such mutations are associated with the occurrence of skin symptoms in ODDD and provide the first evidence for the existence of a genotype-phenotype correlation.

• Authors: M Vreeburg, E A de Zwart-Storm, M I Schouten, R G L Nellen, D Marcus-Soekarman, M Devies, M van Geel, M A M van Steensel
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 143 Issue 4 Pg. 360-3 (Feb 15 2007) ISSN: 1552-4825 [Print] United States
• PMID: 17256797 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: (c) 2007 Wiley-Liss, Inc.

Chemical References

• Connexin 43

Topics

• Abnormalities, Multiple (genetics)
• Adult
• Connexin 43 (genetics)
• DNA Mutational Analysis
• Eye Abnormalities (genetics)
• Female
• Humans
• Keratosis (genetics, pathology)
• Limb Deformities, Congenital (genetics)
• Phenotype
• Sequence Deletion
• Skin Abnormalities (genetics)
• Syndactyly (genetics)
• Tooth Abnormalities (genetics)