van der Harten H J, Brons J T, Dijkstra P F, Niermeyer M F, Meijer C J, van Giejn H P, Arts N F
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
Pediatr Pathol. 1988;8(6):571-97. doi: 10.3109/15513818809022316.
In the classification of lethal osteochondrodysplasias, achondrogenesis and hypochondrogenesis have recently received special attention. We describe 23 cases representing the different subtypes. Within the classical type I (Parenti-Fraccaro) two distinct disorders can be recognized: type IA (Houston-Harris) and type IB (Fraccaro). The classical type II (Langer-Saldino) and hypochondrogenesis represent phenotypic variants of one disorder in which type II is the most severe form and hypochondrogenesis the mildest form, while transitional forms exist. It is likely that a basic defect in cellular function of the chondrocyte results in a deficient cartilage matrix and in disorganized enchondral ossification.