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Achondrogenesis Type IA (Houston-Harris): A Still-Unresolved Molecular Phenotype

2007; SAGE Publishing; Volume: 10; Issue: 4 Linguagem: Inglês

10.2350/06-07-0134.1

1615-5742

Thomas Aigner, Tilman T. Rau, Manuel Niederhagen, Frank Zaucke, Markus Schmitz, Uwe Pöhls, Helmut Stöss, Anita Rauch, Christian T. Thiel,

Cancer, Hypoxia, and Metabolism

Achondrogenesis type IA (Houston-Harris) is an extremely rare lethal chondrodysplasia with a characteristic severe disarrangement of endochondral ossification. The growth plate cartilage completely lacks columnar-zone formation and shows chondrocyte expansion due to intracellular vacuoles. This article on a new case of achondrogenesis type IA confirms these findings and demonstrates, on the ultrastructural level, the retention of fine fibrillar material within the rough endoplasmic reticulum (rER). Molecular analysis in the presented case of achondrogenesis type IA did not reveal mutations in the COL2A1 and SLC26A2 genes, which are known to cause achondrogenesis types IB and type II. Although the extracellular cartilage matrix was severely altered, all of the investigated matrix molecules (collagens, aggrecan, matrilins, cartilage oligomeric protein [COMP]) showed a normal distribution pattern. The only exception was type-X collagen, which was significantly reduced. Overall, our study suggests a disturbance in cartilage matrix assembly in the present case due to the retention of some sort of matrix component within the rER. Presumably, as a consequence of this event, processes of chondrocyte maturation and differentiation and endochondral bone formation are severely affected in this case of achondrogenesis type IA.